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2120 OBITUARY NOTICES. OBITUARY NOTICES. ALBERT ERNEST BELLARS. BORN AUGUST 25~1i 1880; OIED APRIL 23~11 1921. ALBERT ERNEST BELLARS was the son of the late Alderman E. K. Rellars of Wisbech. He was educated at Wisbech Grammar School under Mr. A. W. Poyser and a t Magdalelie College Cam-bridge where he held a Holmes Exhibition. After taking his degree in the Natural Sciences Tripos in 1902 he was appointed Assistant Demonstrator in the laboratory of Gonville and Caius College under Mr. M. Pattison Muir. Later he undertook the supervision in chemistry of students in Gonville and Caius and in Magdalene Colleges. Between 1903 and 1910 he was engaged in research work the results of which have appeared in the Trans-actions of the Chemical Society and in the Proceedings of the Cambridge Philosophicd Xociety .At Cambridge he was an enthusiastic teacher and very popular with students in the laboratory and in the college classes under his supervision. As a colleague in research, he was a skilful and accurate experimenter and he never tired in his determination to solve a problem. No failure disheartened him and his cheery optimism gave stimulus to work in which he was engaged. With the writer he published between 1903 and 1907 the results of four investigations which have appeared in the Transactions. In 1911 after the closing of the chemical laboratory of Gonville and Caius College he wits appointed Professor of Chemis-try a t the Rangoon University College on the recommendation of Sir W. J. Pope and soon proved himself to be a stimulating lecturer and teacher Last year he was appointed the first Professor of Chemistry in the new University of Rangoon.The splendidly-equipped chemical laboratory at University College is a monument to his thoroughness and foresight and a long list of those who have graduated in science in Burma during the last ten years bears testimony to his unwearying labour and to the activity of the interest in that branch of science of which he himself was so keen a student. The claims of teaching work left little opportunity for research until lately when in the new lab-oratory he was able to resume it. Serious throat trouble compelled him to come to England this year for an operation which was a t first successful but a sudden attack of hzemorrhage occurred later, which was fatal.In December 1919 Professor Bellars married Miss Beryl Coxon only daughter of Major Coxon of King’s Lynn OBITUARY NOTICES. 2121 Norfolk. She returned to England with her husband this year and was with him at his death. Professor Bellars leaves a post-humous son born a week after his death. In Burma great sym-pathy is felt for his widow who had been in the colony only a little more than a year when her husband was invalided home. Bellars was a keen sportsman in every sense of the word. At Cambridge he was captain of his college cricket team and played regularly in the Cambridge County Eleven. He was an enthusiastic skater of the fen style and a golfer. In the Long Vacations he was one of the band of climbers of the Alpine Club and was associated with the late Dr.H. 0. Jones in several of his ascents. In the Easter Vacations he climbed in Snowdonia or in the Lake District. While in Rangoon he took a keen interest in all matters connected with sport and volunteering at the University College and officiated regularly a t the local athletic meetings. Bellars was the ideal type of colonial University Professor. The soundness of the knowledge of his subject combined with a driving power and personality commanded the loyalty and respect of his students, not only in the lecture room but also in-the college sports. He was of the true type of teacher and leader of men such as have built up the British Empire and yet he was of a retiring disposition and never sought popularity outside the circle in which his main interests lay.His sudden and early death is much to be deplored. He was devoted to his work and to his home. R. S. MORRELL. EDWARD JOHN BEVAN. B O ~ N DECEMBER ~ I T H 1856; DIED OCTOBER ~?TH 1921. EDWARD JOHN BEVAN son of Edward Bevan of Birkenhead was born in 1856. After a private school education he received a training in chemical science which may be described as irregular. Beginning a t the age of seventeen with the routine of laboratory control of alkali processes in the service of the Runcorn Soap and Alkali Co. he made friendships with certain pioneer workers in that industry who usefully influenced his career by advising sys-tematic training a t the Owens College-then a leading centre of research. The meet'ing with C. F. Cross resulted in a student friendship which developed into one of collaboration both leaving the College (1879) to undertake research work in the cellulose industry Bevan's sphere being that of paper-making.Problems of common interest were investigated of which results were pub 2 122 OBITUARY NOTICES. liahed in the Journal of the Chemical Society (1882). It was already evident that the field of work entered on promised results in pro-portion to industry; it w~ decided to make a definite adventure, and “ Cross and Bevan,” migrating to London were able to find a provisional working home in the Jodrell Laboratory Kew through the friendly offices of H. E. Armstrong Hugo Muller and Thiselton-Dyer. The scope of research widened to include the physiology of the vegetable fibres the equilibrium of the fibre substances as chemical individuals in relation to water-oxygen conditions hence a special study of cellulose reactions with hydrolytic agents and oxidants ; and in development of the natural history aspect of the subject, the working out of a comprehensive scheme of analysis of the fibres and fibre-aggregates the raw materials of the textile and paper-making industries.The scientific data thus accumulated were then applied in de-veloping industrial inventions such as the bisulphite process of treating wood for the preparation of cellulose (“ pulp ”) then in its infancy and pioneered in this country by C. D. Ekman and textile bleaching processes for example those of Thompson, Hermite (electrolytic) and W. Mather.The Colonial and Indian Exhibition provided a sphere of active work in vegetable fibres, and established the method of analysis and evaluation of these raw materials as a “standard,” subsequently to be generally accepted as such. Concurrently with these technical activities, the systematic research work on cellulose and its derivatives was followed up and investigations of alkali-cellulose (mercerisation) and benzoates (Baumann’s method) led in logical sequence to the discovery of the xanthogenic hydrate-ester series of derivatives, patented in the joint names and the basis of the now we1l;known “ viscose ” industries. The formal partnership “Cross and Bevan,” and its establish-ment at New Court Lincoln’s Inn (1885) led to outside activities, such as those connected with patent litigation in which Bevan showed his exceptional abilities and decided leanings to the pro-fessional side of chemical science.Applying for the post of Public Analyst under the Middlesex County Council he was appointed (1892) and held the office to the date of his death. As necessary incidents of this position he became progressively influential in the Society of Public Analysts of which he was sometime President, and on the Council of the Institute devoting himself with his usual thoroughness to its interests and high aims. Bevan’s career expresses his whole-hearted devotion to Science, for his varied activities were all marked and hall-marked by th OBITUARY NOTICES. 2123 Bevere discipline of the pursuit of “ the Truth ” as “ the whole Truth and nothing but the Truth,” as we chemists know the truth of an experimental science with the uncompromising laws under which we work for its establishment.With these qualities were associated those which express them-selves in good fellowship. Bevan was popular as he was genial and generous. His surviving relatives treasure the many expres-sions of affection and regard contained in letters from his brother chemists. For a complete and chronological record of the publications in which Bevan was associated with the writer those who may be interested are referred to the Paper TTade Review of January 28th, 1921. c. E”. CROSS. EDWARD KINCH. BORN AUGUST 1 9 ~ ~ 1848; DIED AUUUST ~ T H 1920. EDWARD KINCH was born a t Henley-on-Thames and was educated a t the Grammar School there.His father Charles Kinch was a pharmaceutical chemist and would seem to have been a very energetic man for he also had a printing and stationery business, published a local paper and took an active part in the management of the affairs of the town. Although Edward Kinch spent his early life there it is not in association with Henley that one thinks of him but with that agricultural district on the Upper Thames where the counties Berkshire Wiltshire Oxfordshire and Gloucestershire meet. There on the Berkshire bank of the Thames lies the scattered village of Eaton Hastings and at the “ Grange,” a charmingly old-fashioned somewhat rambling farmhouse many generations of the Kinch family had dwelt and farmed their own land whilst. relations of theirs were to be found in many of the large farms in the district lying between Farringdon and the Cotswolds.Amongst them were men who have made their mark in agriculture such as Charles Hobbs of Maisey Hampton and his son Robert Hobbs of Kelmscott, both so well known as successful breeders of sheep. It masy be mentioned incidentally that the picturesque Manor House at Kelms-cott standing opposite to Eaton Hastings on the Oxford bank of the Thames which figures so much in the art annals of the Victorian era as the home of William Morris and for a time also of D. G . Rossetti belonged to a widowed aunt of Edward Kinch who lived with her brother William at the Grange. It was in his frequen 2124 OBITUARY NOTICES. visits to these relations probably that Edward Kinch acquired that interest in agriculture that became the dominant feature in his life.On leaving school Kinch went to the Royal College of Chemistry in Oxford Street where he studied for some years under Prof. (later Sir Edward) Frankland. His first appointment (1869) was that of chief assistant to Prof. (later Sir Arthur) Church at the Royal Agricultural College Cirencester and thus began the connexion with the institution with which later he was so intimately associated. He held this post until the latter part of 1872 ; he then joined the staff of the Royal College of Chemistry which with some sections of the Royal School of Mines,,had just been transferred to the new buildings in the Exhibition Road South Kensington to form the nucleus of that institution which after many changes of name is now known as the Imperial College of Science and Technology.After some years spent in teaching in these laboratories Kinch for about a year held the position of Superintendent of Minerals at the India Museum South Kensington. In 1876 he accepted the post of Professor of Chemistry a t the Imperial College of Agriculture, Komaba Taky~ Japan in the organisation of which he took an active part. At this time Japan was still in large part closed to Europeans but in the college vacations Kinch was allowed to travel freely about the country and had opportunities such as fell to few others of seeing “ Old Japan.” One considerable drawback, however was that in many of the out-of-the-way districts it was impossible to supplement in any way the meagre vegetable diet of the natives-the result to a European being semi-starvation.In 1881 Kinch returned to England on his appointment as Professor of Chemistry a t the Royal College of Agriculture Ciren-cester a post which he held until the closing down of the College in 1915 on account of the war. Prof. Kinch married in 1889 Edith daughter of the Rev. George Huntingdon vicar of Tenby but their happy married life was terminated by her death a year later. On the closing of the Cirencester College Kinch retired from active life and went to live at Haalemere where he occupied himself with his garden and with Japanese art a subject in which he was greatly interested. His residence in Japan had enabled him to form a small but admirable collection of curiosities and art work.A serious illness in 1918 left him with very impaired health and he died on August 6th 1920. Edward Kinch was a man who devoted himself heart and soul t o his students and to the interests of the Royal Agricultural College, Cirencester where he spent thirty-four years of his life. Singularly unassuming and of very retiring nature he was beloved by thos 0 €3 ITU ARY N 0 TIC E S . 2125 who came under his influence and the fruits of his sound and careful training of his students were manifested by many of them in sub-sequent spheres. It was for his college and his students that he lived and it was in this connexion rather than in public life or in written contributions to science that he excelled. His principal literary contribution was the revision and practical re-writing in 1906 of the weli-known book for agricultural students “ Church’s Laboratory Guide,” of which a ninth edition appeared in 1912.Occasional papers from him have also appeared in the Journals of the Chemical Society the Royal Agricultural Society and the Surveyors’ Institute but most of his contributions were given in the Agricultural Students’ Gazette issued from the Cirencester College. Kinch was a sound rather than a progressive chemist and a teacher, rather than an investigator but he was a man held in much esteem by those who knew him. In conclusion the words of a former student Lord Bledisloe intimately acquainted with the affairs of the College may be quoted “ If and when the worthy history of England’s premier agricultural college comes to be written no name will rank higher in its annals than that of Edward Kinch and no one will be deemed to have wrought a more beneficial influence in promoting the high reputation of the College and the progress of Agricultural Science in the British Empire.” Prof.Kinch served on the Council of the Chemical Society 1887-1892; a t an earlier period 1872-1875 he was on the Journal staff as an abstractor in Agricultural Chemistry. A. J. G. HENRY RONDEL LE SUEUR. BORN JANUARY IST 1872 ; DIED JULY gTH 1921. H. R. LE SUEUR was born a t Trinity Jersey on January lst 1872, the son of F. C. Le Sueur. He was at a private school until 1887, after which he spent two years in the laboratory of a Jersey analyst, Mr. F.W. Toms and then entered University College London, taking the Honours Chemistry course. He graduated B.Sc. of London University in 1893 and obtained the D.Sc. degree in 1901. He was a Fellow of the Institute of Chemistry (Associate 1898) and a member of its Council from 1914 to 1917 a Fellow of this Society (1895) a member of Council (1907-lgll) and at the time of his death was one of its Secretaries. After graduating in 1893 Le Sueur spent one year in carrying out research work on the properties of dehydracetic acid (Colli 2126 OBITUARY NOTICES. and Le Sueur T. 1894 65 254) and in the following year took up a junior teaching post in the Medical School of St. Thomas’s Hos-pital. Possessing the faculty of imparting knowledge to others, Le Sueur rapidly developed into a teacher of the very first order, and it is a remarkable fact that one possessing such pronounced capabilities in this direction should have remained attached to this one Institution for the twenty-seven years of his career.The writer is well acquainted with the happy atmosphere of St. Thomas’s, and no doubt this weighed with Le Sueur especially as from 1904 he occupied the senior teaching post but it is none the less strange that his exceptional teaching capacity was not more generally recognised. There was only one break in the twenty-seven years during which Le Sueur was connected with St. Thomas’s namely that caused by the War. He was gazetted major Royal Engineers in 1915 and with Major J. T. Hewitt was ordered to Gallipoli to watch and advise on possible developments in gas warfare.There can be little doubt that the illness which he contracted there seriously undermined his health for he was never in reality the same high-spirited man again. On his return to England after being in hospital in Egypt he became one of the chief experimental officers at the R.E. Experimental Station Porton where he was attached until the end of 1917. He was then ordered to the United States to assist in the preparation of the American Gas Warfare Experi-mental Station and he remained there until after the signing of the Armistice. As a research worker Le Sueur was not prolific his total published papers amounting to twenty-four ; this is largely accounted for by the fact that research was regarded by him as a pleasurable relaxation from his teaching duties which always came first.He thoroughly enjoyed every minute he was able to devote to experi-mental work but when accumulated results made the writing of a paper desirable he was very *obviously bored. His researches concerned mainly the fatty acids and their hydroxylated deriv-atives and may be divided into three groups. In one he studied the action of heat on the a-hydroxycarboxylic acids and showed that it is possible t o descend the series of fatty acids step by step, according to the scheme R*CH,*CO,H -f R*CHBr-CO,H -+ R*CH(OH)*CO,H -+- RCHO -+ R-CO,H. ,A somewhat similar process led in a second series of experiments to a simple method for the preparation of secondary amines thus R*CHBr*CO,H -+ R*CH(NHAr)*CO,H --+ R*CH,*NHAr + CO, whilst the third group of researches on the action of fused potassium hydroxide on the dihydroxy-acids obtained by oxidation in the oleic acid series OBITUARY NOTICES.3127 revealed an unusual transformation namely the movement of a heavy radicle within the molecule of an aliphatic compound. The change is represented thus R*CH(OH)*CH( OH)*[CH,],*CO,H -+ OH*CH,*CR( OH)*[CH,],*CO,H -+ CO,H*CR(OH)fCH,],*CO,H. The elucidation of the constitution of the hydroxydicarboxylic acids formed in this way led incidentally to the discovery of heneicosoic acid a missing member of the simple fatty acid series. In manner Le Sueur was quiet and reserved not to say shy; few knew him well for his efforts to disguise the above characteristics sometimes gave quite a wrong impression of the real man.His great outstanding quality was loyalty which governed his every action and was one of the main causes of the loving regard in which he was held by his intimate friends. As a Jerseyman Le Sueur had an iatense feeling of local patriotism and his friends knew well his loyalty to the “ Duke of Normandy.” He was one of the founders of the Jersey Society in London and one of its most active members during more than twenty years being chairman of its council at his death. He spoke a dialect of the ancient Norman-French language fluently and with historical pride and it was because of his love for his native land that he desired to be laid to rest in Jersey. A. W. CROSSLEY. GEORGE BLUNDELL LONGSTAFF M.A. M.D. (OXON.), F.R.C.P.F.S.A. F.L.S. F.C.S. F.G.S. J.P. BORN FEBRUARY 12TH 1849; DIED MAY 7TH 1921. IN the late George Blundell Longstaff the scientific the artistic, and the practical temperaments were so nicely blended that it would be impossible to say which of these qualities preponderated in his attractive and versatile nature. Those who made his acquaintance as a field naturalist and had occasion to note his keen powers of observation his untiring activity as a collector, and his readiness to appreciate the scientific bearing of the facts that he and others accumulated might not unnaturally be surprised to find that his technical knowledge of the building craft was the admiration of experts and that his judgment on all matters of the graphic and plastic arts was highly valued by the most experienced critics.It is interesting to call to mind that many of the most con-spicuous traits in Longstaff’s character may be traced back to his ancestry. Thus his father in early days an associate of “ Osmotic Graham,” was noted for his devotion to chemistry; to the Dixo 2128 OBITUARY NOTICES. strain may be attributed his interest in everything practical and constructive ; while the extraordinary energy with which he worked a t entomology may be considered not improbably to be fore-shadowed in the stock from which sprang Spence of “Kirby and Spence. ” Born a t Wandsworth in 1849 Longstaff was the second son of Dr. George Dixon Longstaff and of Maria daughter of H. Blundell, of Hull. At Rugby he came under the influence of Archbishop Temple then Headmaster and of Archdeacon J.M. Wilson then Master in Natural Science and Mathematics. Each of these great teachers left a strong impress on the mind and character of their pupil. Proceeding in due course to Oxford he gained a scholarship in Natural Science a t New College following this up with a First Class in Natural Science. It was while an undergraduate a t Oxford that by a deplorable accident he lost the sight of an eye. Through-out his life the condition of his sight was such as to necessitate the greatest care in the use of his remaining eye; and he was com-pelled to forego many schemes of scientific research which his inclina-tions would have led him to adopt. But he faced his misfortune with admirable courage and engaged with vigour and energy in all the pursuits of a kindred nature which still remained open to him.After taking his degree in Arts he entered at St. Thomas’s Hospital and having passed through his career as a medical student with distinction he graduated as M.B. subsequently as M.D. a t Oxford ; and obtained the Membership eventually the Fellowship, of the Royal College of Physicians. In 1875 he married a daughter of Edward Dixon of Southampton a member of n family already connected with his own. The intellectual endowments the philan-thropic ideals and fine taste of this lady were most congenial to him and it would have been difficult to find a better-assorted couple. On settling down with his wife and young family first at Wands-worth and afterwards on Putney Heath he devoted himself to the study of preventive medicine and vital statistics paying special attention to all such matters as might benefit the conditions of life among the poorer and less fortunate members of the community.The present writer became associated with him in some of this early work especially in the investigation of the properties of a much-advertised germicide and in the statistical aspects of various diseases. This led to a long collaboration in the Registrar-General’s Department at Somerset House many results of which saw the light in his published volume of “ Studies in Statistics.” Whilst still engagedein work of this kind he acquired the beautiful estate a t Mortehoe in North Devon where much of his subsequent life was passed and where he threw himself with characteristic energ OBITUARY NOTICES.2129 into the study of the history antiquities natural productions and social conditions of that part of the county. To these rural pur-suits he added much varied activity in London serving on the London County Council as member for Wandsworth from 1889 to 1903; and as Chairman of the Building Act Committee of that body taking a principal part in the drafting and passing through Parliament of the London Building Act 1894. As J.P. both for London and Devon he gave much time to magisterial duties and as Guardian of the Poor he found scope for the exercise of his interest in the social conditions of the more indigent classes. It had always been his desire to travel ; and he soon found oppor-tunity to acquaint himself with many remote parts of the earth.At different times he visited Madeira the Canary Islands Algeria, Egypt and the Soudan South Africa India Ceylon China Japan, North and South America the West Indies A4ustralia and New Zealand. In all of these places he made large collections prin-cipally of insects and recorded numerous observations of high interest in the elucidation of bionomic questions. The results of these labours in the field of natural history were published by him in several important memoirs collected some’ nine years ago in a volume entitled ‘( Butterfly Hunting in Many Lands.” The insect collections which are of great value both in themselves and for the exact data by which each specimen is accompanied were presented by him to the Hope Department in the University of Oxford.This Department found in him a generous and far-sighted benefactor ; it being indebted to him amongst other donations, for an endowment of f2400 for the provision of an additional assistant. Beside aIl his other avocations he found time to take an active part in the work of the Charity Organisation the Royal Statistical and the Entomological Societies being a t various times Vice-president of the latter two. He was also a Fellow of the Linnean and Geological Societies of the Society of Arts and of the Chemical Society. In the last-named he took a special interest, and in the year 1916 to mark the seventy-fifth anniversary of the Society he made over to it the sum of f 1000 for its Research Fund ; thus following the example of his father who in 1876 had given flOOO to establish this Fund.A “Longstaff Medal” is awarded by the Council of the Society every three years for the best series of original investigations in chemistry published in England, Longstaff’s munificence was not confined to scientific objects ; for many schemes of social improvement were helped by him with ample donations and he was a liberal benefactor to the Church. He was especially concerned in the planning and building of the new church a t Woolacombe North Devon; and the ancient churc 2130 OBITUARY NOTICES. of Mortehoe bears many marks of his generosity; in particular a beautiful stained-glass window by his friend Selwyn Image lately Slade Professor of Fine Art at Oxford. Three years after the death of his first wife he married Miss Donald a daughter of the late M.H. Donald of Stanwix and Blaith-waite Co. Cumberland a lady distinguished for her attainments in conchological science and with many interests similar to those of her husband. A man of such varied capacities and of so generous and sym-pathetic a nature as George Blundell Longstaff was sure to have numbers of attached friends by whom his death is felt as a grievous personal loss. His memory will be widely cherished as that of an inspiring and stimulating companion and one of the most considerate and open- handed benefactors of his generation. F. A. D. EDMUND JAMES MILLS. BORN DECEMBER 8TH 1840; DIED APRIL 21ST 1921. PROF. E. J. MILLS who died on April 21st 1921 was born in London on December 8th 1840.He was educated fist at the Grammar School Cheltenham and then at the Royal School of Mines where he took the courses of instruction for a degree in science at London University at that time the only university in Britain granting such degrees. He graduated B.Sc. in 1863 and obtained the doctorate in 1865. There were few candidates for science degrees at that time and on looking a t the List of graduates it is interesting to note that Mills’s name appears about equidistant in time between those of Prof. Alex. Crum Brown in 1862 and Sir William Tilden in 1871. In 1861 Mills became assistant to Dr. John Stenhouse and a year later he was appointed one of the demonstrators in chemistry at Glasgow University in which capacity he conducted tutorial classes for medical students a work not very congenial to him and one for which from his temperament he was not particularly well fitted; he was however a good laboratory teacher for advanced students.He resigned this appointment in 1865. In 1875 Mills became superintendent of the ‘‘ Young Laboratory,” in Anderson’s College Glasgow and during his term of office about the year 1886 that foundation together with Anderson’s College became incorporated in the Glasgow and West of Scotland Technical College the Young Laboratory appointment being converted int 0BITUAR.Y NOTICES. 2131 the Young Chair of Technical Chemistry. His predecessors in charge of the Young Laboratory were W. H. Perkin sen. 1870-71, and G. Bischof 1871-75. Mills was the author of many papers covering a wide field of work.Although his first recorded paper in the Proceedings of the Royal Society (1860) is upon bromo- and chloro-phenylamine his early work inclined more to general and inorganic chemistry, dealing with subjects such as isomerism statical and dynamical ideas on chemistry chemical equivalents etc. and this tendency is seen also in his later papers in the Philosophical Magazine pub-lished during 1883 1884 and 1887. In the Journal of the Chemical Society his more important papers are :-“ On Aniline Derivatives and Nitrotoluene ” (1875-76) ; “ On Potable Waters ” (1878-81) ; ‘( On Chemical Repulsion ) ) (1880-81) ; “ Melting-points ” (1882). From 1879 to 1882 he published “ Researches on Chemical Equiva-lence ” ; from 1878 to 1880 papers on “ The Action of Oxides on Salts ” ; and later “ Researches on Dyeing,” in conjunction with Louis Campbell.To the Society of Chemical Industry he con-tributed papers on the < < Quantitative Estimation of Oils and Pats )’ (1883) “ Viscosity Determinations ” (1886) and “ Oxida-tion of Aniline )’ (1894). In his books Mills did not confine himself to purely scientific matters; for in addition to two works “Fuel and its Applications” (published conjointly with E. J. Rowan in 1889) and ‘( Destructive Distillation ” (1892) he wrote a volume of poems “ My Only Child ” (1895) and “ The Secret of Petrarch ’) (1904). Mills was elected a Fellow of the Royal Society in 1874 and was an honorary LL.D. of Glasgow University; he was an original member of the Society of Chemical Industry and served on the committee of the Glasgow Section including two periods as vice-chairman from 1884 to 1894; and was a member of the Council of the Chemical Society at various times from 1868 to 1906 serving as vice-president from 1912 to 1915.Mills returned to London finally settling at West Acton. He spent much of his leisure time in the practice of photography in which he was a skilled manipulator. He attended many of the meetings of the Scientific Societies to which he belonged and rendered valuable service to the Chemical Society as a member of the Library Committee in which he took special interest. J. M. T 2132 OBITUARY NOTICES. RICHARD HENRY VERNON. BORN JANUARY Z~TH 1885; DIED APRIL’ ~ T H 1921. RICHARD HENRY VERNON was the elder son of the late Hon.William Vernon son of the sixth Baron Vernon and of Mrs. Vernon daughter of the late General Daniel Marsh Prost of St. Louis City U.S.A. Born in London at 12 Clarges Street Vernon had a serious illness a t the age of nine which left consequences that made it doubtful whether he would be able to stand the English climate. He was therefore educated in Switzerland. He entered the gcole Cantonale at Lausanne in 1898 and proceeded to the Gymnase Scientifique, which he left with the Certificat de Maturit6 in 1902. Here he showed powers of work and a capacity for scientific and mathematical subjects which won the highest opinion from his teachers. It had always been his father’s desire that he should receive an American University education and a t the age of nineteen he entered a t Cornell.He was then full of high spirits and love of adventure and it was there that he won a bet that he would walk sixty miles in twenty-four hours. He covered the distance with two hours to spare although it was in winter and the walk had to be made in the snow. However he found the environment at Cornell uncongenial. The free open-air life of the Western States had an irresistible attraction for him and to the concern of his parents he broke off his University career and went to California, where a maternal uncle had an estate. Here he learnt all the craft of the ranch-afterwards a t Cambridge he would sometimes amuse his friends by illustrating with a rope some of the skill that he had acquired with the lariat-and for some time he lived an independent life maintaining himself as “ broncho-buster ” and cowboy.Drifting in this way from California t o Texas he came a t length to the little township of Throgmorton. Here there was a school-master who had some knowledge of physics and with him Vernon became very friendly. The two used to discuss scientific problems together and Vernon was made by him to realise that he had gifts which were being wasted in the life he was then leading and was persuaded to return to Europe to continue his education. His parents were at Wiesbaden and he joined them there and spent six months working in the laboratory of Professor Fresenius. Presenius recognised his ability and encouraged him to take up chemistry as a profession.Accordingly in 1907 at the age of twenty-one he entered the Eidgenossische Technische Hochschule a t Zurich where after working through the customary four years’ course in chemistry physics and mathematics he obtained th OBITUARY NOTICES. 2133 diploma in 1911. He then began under the direction of Prof. F. P. Treadwell the work on the electric conductivity of very pure water which was to form the subject of his thesis for the doctor’s degree. The greater part of this thesis is occupied with the calcula-tion of the relations between the inductances and capacities of the arms of the Wheatstone bridge which give the sharpest minimum of sound in the telephone. He demonstrated the practical utility of arrangements based on his results and employed them to examine the methods of obtaining pure water by distillation.After receiving his doctor’s degree in the spring of 1914 he began a magneto-chemical investigation of platinum compounds with Prof. Pierre Weiss but this was cut short by the events of the following August. He was then fishing in the Black Forest and barely succeeded in crossing the frontier a t the declaration of war. He hastened to England t o offer his services but was rejected several times on account of eyesight. Ultimately he enlisted in the R.A.M.C. but a.fter serving for a short time with that corps he was transferred to the Royal Engineers where he became a despatch rider. In 1916 he was granted a commission in the 3rd Battn. of the Dorset Regiment and in the spring of 1916 proceeded to the Western Front where he saw much active service chiefly in the Armentihres district and on the Somme.After two long periods of illness in hospital he was pronounced unfit for active service and was trans-ferred for duty to the Chemical Warfare Committee for whom he worked first a t the Imperial College of Science in conjunction with Prof. Baker on dichlorodiethyl sulphide and afterwards a t Cam-bridge in the University Chemical Laboratory where a t the suggestion of Sir William Pope he began an investigation of the allcyl tellurium compounds. In July 1918 Vernon was sent as Chemical Adviser to the Shell Filling Factory a t Chittening. Here he rendered services of the greatest value in contriving precautions to be taken in the handling of “ mustard gas,” in working out methods for cleaning up spills and rendering the waste innocuous and in training the operatives in the use of the measures which had been devised.It fell to him to grapple with the mischances that not infrequently occurred. When for example as happened in the early days of the factory a defective cock led to a spill of several gallons it was the Chemical Adviser who had to deal with the emergency. He won the regard and confidence both of the staff and of the operatives; the men of his special anti-gas detachment in particular gave him willing and loyal support. Life in the factory a t f i s t was rendered intolerable by the vapour of the “ mustard gas,” which permeated everything ; sometimes in fact before the later improvements were introduced 2134 OBITUARY NOTICES.the whole of the workers in a shed would be left on the sick list at the end of a four hours' shift. It was largely through the devotion, and indeed the heroism of the Chemical Adviser that in spite of everything the factory was able to send out in a steadily increasing stream the shells so urgently needed to enable the troops in the field to reply to the deadly weapon which the enemy had adopted. By the continuous strain of work such as this Vernon's health was severely tried and a t the time of the Armistice he was in hospital very dangerously ill with pneumonia. After a period of convales-cence in the south of France he was able to return to Cambridge, and in the spring of 1919 he entered Gonville and Caius College as a research student and resumed his work on the tellurium compounds.Before going to Chittening Vernon had prepared a number of dimethyltelluronium derivatives. He now examined more closely the base formed by treating dimethyltelluronium iodide in aqueous solution with silver oxide and thus made the highly interesting discovery that when the solution of this base is evaporated to dryness a new base is produced the salts of which are isomeric with those of the original series. As a difference of structure seems excluded the two series of salts are almost certainly stereoisomeric. Vernon's observations indicate therefore that in dimethyltellur-onium iodide the four radicles about the tellurium atom have not a regular tetrahedral arrangement as might have been anticipated, but lie more or less in one plane.a-Iodide. a-Base. P-Base. /%Iodide. According to this view the u-salts and a-base are trans-compounds, the p-sa,lts are cis-compounds and the displacement of the methyl groups on heating the a-base is due to the fact (for which some experimental evidence was obtained) that the p-base is an oxide. The marked analogy which this formulation indicates between the configurations of the dimethyltelluronium iodides and those of platosamminochloride and platosemidiamminochloride as inter-preted by Werner is very suggestive. This work the results of which are published in four papers in the Society's Transactions (T. 1920 117 86 889; this vol. p. 105 OBITUARY NOTICES. 2135 687) occupied Vernon until Christmas. For it he was awarded the certificate of research of the University and in due course took his B.A.degree. During the Christmas vacation which he spent at Montreux he was attacked with another serious illness and in consequence had to undergo a severe abdominal operation so that he was unable to return to Cambridge until Easter 1920. He was then appointed to the official position in the University of Assistant to the Professor of Chemistry and began in conjunction with Sir William Pope and Mr. F. G. Mann a detailed experimental investigation of the inter-action of ethylene and sulphur monochloride (this vol. p. 634). During the next few months his health to external appearances, improved greatly and he seemed to have made a complete recovery from the operation at Montreux but in the l a b autumn disturbing symptoms of arterio-sclerosis brought about by the kidney disease left as a consequence of his early illness showed themselves and increased in gravity through the early months of the present year. He sank very rapidly at the end and died on April 9th 1921 at the age of thirty-six. Although Vernon had been at Cambridge for comparatively so short a time he had gained the a$ectionab regard of many of the senior members of the University as well aa of the younger men for his personality was one of singular charm and attractiveness that rapidly won the friendship of all with whom he was more closely associated. His education had been so different from that of the men whom he met in the laboratories and colleges &s to give him a fresh and often unconventional outlook on the questions that arose, and the engaging frankness with which he would state his views made him always an interesting companion. As a chemist he was gifted with quite exceptional experimental skill. All who were familiar with his methods of work were grea,tly impressed with his powers and know that through his untimely death an investigator of unusual promise has been lost. W. H. M

ISSN:0368-1645    

DOI:10.1039/CT9211902120

出版商:RSC    

年代:1921

数据来源: RSC

摘要:

INDEX OF AUTHORS' NAMES. TRANSACTIONS. 1921. A. Abney (Sir) TP'illiam de Wiveleslie, obituary notice of 529. Aldous Wilfrid Major. See iVevil Vincent Sidgwick. Alimchandani Rupehand Lilaranz and Andrew Norman Xeldrum derivatives of gallicncid. Part 11. Gallic acid (and the cresotic acids) and chloral, 201, Allmand Arthur John. See Hubert Thoman Stanley Britton. Allpress Charles Frederick. See Frederick Challenger. Andrewe (Miss) Alberta Catherine Pritchnrd. See John Read. Aston Francis William mass-spectra and atomic weights 677. Atack Frederick William the structural isomerism of the oximes. Part I. Criticism of the Hantzsch-Werner hypothesis and a new theory of the constitution of isomeric oximes 1175. Atack Frederick WilZiam and Leonard Whinyatea the structural isomerism of the oximes.Part 11. A fourth benzildioxime 1184. B. Baokes John Valentine Ralph Winton West and (Miss) Martha Annie Whiteley quantitative reduction by hydriodic acid of halogenated malonyl derivatives. Part I. The amides and s-di-alkyl and -aryl substituted amides of mono- 'and di-bromomalonic acid 359. Bagster Lancelot Xalisbury the re-action between nitric acid and copper, 82. Baker Julian Levett and Henry Prancis Everard Hulton aniylases of the cereal grains-rye 805. Bakr Abu Hohamsd and Joseph Edgar King the determination of the sorption of both solvent arid solute. Part I. Preliminary ; the system : benzene-iodine-charcoal 454. CXIX. Baly Rdward Charles CyriZ and William Francis Barker the photo-chemical reaction between hydrogen and chlorine and its variation with the intensity of the light 653.Baly Edward Charles Cyril Isidor Horris Heilbron and William Francis Barker photocatalysis. Part I. The synthesis of formaldehyde and carbohydrates from carbon di-oxide and water 1025. Barker William Francis. See Edward Charles Cym'l Baly. Barnett Edward de Barry and James Wilfred Cook studies in the anthracene series. Part I. 901. Barrow Fred and Evan Dalton Griffiths condensation of p-nitko-benzyl chloride with nitroso-com-pounds; a new mode of formation of N-oximino-ethers 212. Barrow Pred. See also AEexunder McKenzie. Bassett Henry obituary notice of, 532. Bassett Henry jun. and Thomas Arthur Simmons the system picric Bassett Henry jun.See also Lawson John Hudleston. Bellarra Albert Brnest obituary notice of 2120. Bennett Geoyge MacdonaZd BB'-di-chlorodiethyl disulphide 418. Bennett George Macdonald and (Miss) Edith Muriel Whincop some deriva-tives of monothioethylene glycol, 1860. Bevan Edward John obituary notice of, 2121. Bhatnagar Shanti Swarupa studies in emulsions. Part 11. The reversal of phases by electrolytes and the effects of free fatty acids and alkalis on emulsion equilibrium 61. studies i n emulsions. Part 111. Further investigations on the re-versal of type by electrolytes, 1760. * acid-5-phenylacridine 41 6. 4 2138 INDEX OF AUTHORS. Birch Stanley Framis William Henry Gough a d George Armand Robert Kon the formation and stability of spiro-compounds.Part VI. New derivatives of cyclopropane and cyclo-hexanespirocyelupropane 1315. Blount Bcrtyam obituary notice of, 545. Blyth AZexai$cr TVyiiter obituary notice of 54.6. Boeree Alfred Reginald. See Henry Thomas Tizard. Bone William Arthur and Leonard Silver a new method for determin-ing the volatile matter yielded by coals up to various temperatures, 1145. Bonnell (Miss) Jane and Edgar Philip Perman the colour of iron alum, 1994. Bowman John Herbert. See Oscar Lisle Brady. Boyle John Scott Walker. See Alexander McKenzie. Brady Oscar Lisle and Johr Herbert Bowman dinitrotolylhydrazines 894. Brady Oscar -Lisle and William Howieson Gibson 2:4:6-trinitrotolyl-methylnitroamine 98. Briggs Samuel Henrg Cliford valency and co-ordination 1876.Britton Hubert Thomas Xtadey the solubility of glucinnm sulphate in water and sulphuric acid a t 2 5 O , 1967. Britton Hubert Thomas Stanley and Arthur John. Allmand the system: potassium sulphate-glucinum snlph-ate-water‘at 2 5 O 1463. Bronsted Johaitnes Xicolaus the in-fluence of salts on chemical equilibria in solutions 574. Buck Johannes Sybrandt. See Isidor Morris Heilbron. Burgess Hewy. See Gilbert Thomas l o r g a n . Buroett Robert AZcxnnder. See John Arnold Cranston. Burrows George Joseph the rate of hydrolysis of methyl acetate by hydrochloric acid in solutions con-taining sucrose 1798. Burrows Gcorye Joseph and Exstace Ebe?icxer Turner experiments on the production of compounds con-taining arsenic as a centre of optical activity 426.some additive compounds derived from arsines 1448. the constitution of the nitroprnssides. Part 11. The alkylation of nitro. prussic acid 1450. )urton IIwoltl and James Kenner, the influence of nitro-groups on the reactivity of substituents in the benzene nucleus. Part 111. The partial recluction of the dinitro-toluenes by stannous chloride and hyclrochloric acid 1047. iutler Gerald Snowden. See Horace Barratt Dunnicliff. C. kin John Cannell obituary notice of, 533. :ashmore Albert Eric IIamilton IcCombie and Harold Archibald Scarborough the velocity of reaction i n mixed solvents. Part I. The velocity of saponification of two ethyl eaters in ethyl alcohol-water mixtures, 970. Xallenger Frederick and Chades Frederick Allpress organo-derivatives of bismuth.Part IV. The interaction of the halogen derivatives of tertiary aromatic bismuthines with organo-derivatives of magnesium and mercury, 913. :hallenor William Arthtcr Perciral. See Gilbert Thomas Morgan. :hapman William Ronald the propa-gation of flame in mixtures of ethylene and air 1677. Chattaway Frederick DanieE and Francis Earl Ray the decomposition of tartaric acid by heat 34. Clapham Heitry William. See Harry Repworth. Clendinnen Frederick William Jefrey, and Albert Cherbtiry David Rivett, the ternary system arnmoniuiri chlor-ide-manganous chloride-water 1329. Coffey Samuel the action of the chlor-ides of sulphur on substituted ethylenes ; the action of propyl-ene on sulphur monochloride and the synthesis of BB’-dichlorodi-n-propyl sulphide 94.the mechanism of the oxidation of drying oils as elucidated by a study of the true oxygen absorption. Part I. Linseed oil and its fatty acids 1152. linolenic and hexabron~ostearic acids and some of their derivatives 1306. the mechanism of the oxidation of drying oils as elucidated by a study of the true oxygen absorption. Part 11. LinoIenic and linolic acids, 1408 INDEX OF AUTHORS. 2139 Obffey Samuel and Charles Frederick Ward the preparation of some ally1 compounds 1301. Cohen Julius liereid and Herbert Grace Crabtree structure and colour of the azine scarlets 2055. Cohen JzJitts Berend. See also Victor Proelicher John IWiard Scott and Akira Shimomura.Collie John NormaqL and (Miss) Amy Ada L’eatyice Reilly a new type of iodine compound 1560. Cook James ZVdjrcd. See Ediuard cle Barry Barnett. Copisarow Maurice the Friedel-Crafts’ reaction. Part 111. Migration of allryl groups in the benzene nucleus, 1806. Copisarow Maurice [with Cyril Norman AuyJt Long] the Friedel- Crafts’ reac-tion. Part 11. Migration of halogen atoms in the benzene nucleus 442. Cox Henry Edward the influence of the solvent on the temperature-coeffi-cient of certain reactions ; a test of the radiation hypothesis 142. Crabtree Herbert Gyace. See Ju lilts Berend Cohen. Oraneton Johit Arnold and 12obert Alexander Bnrnett the adsorption of thorium-B and thorium-C LIY ferric hydroxide 2036. Crompton Holtand and (illiss) Phyllis Xary Triffitt dichloroacetates and chlorobromoacetates from a@-dichloro-vinyl ethyl ether 1874.Croasley Arthw William and (Miss) Nora Renouf 1:l -dimethylcyclohexane from methylheptenone 271. D. Davies William tho cnmulative effect of tlie chlorine atom and the riiethyl and sulphonyl chloride group on substitution in the benzene nucleus. Pitrts I. and II. 853 876. Denham William 87sinith the methyl-lation of cellulose. Part 111. Homo-geneity of product and limit of metliylation 77. Doubleday (Miss) Ida. See Torn Sidney Moore. Drew Harry Bugald Keith. See Gilbert Thomas Morgan. Driver John and Jamw Brierley Firth, the sorption of alcohol and water by animal charcoal 1126. Druce John Gerald Frederick. ethyl-stannic acid and derivatives 758.Dudley Harold Ward ainin oacy lcholin e esters. Part I. Glycylcholiue 1256. Dnff Ja?nes Cooper complex metallic ammines. Part V. cis-8uccinatodi-ethylenediaminecobaltic salts and other cobaltamminc salts containing a seven-membered ring in the com-plex 385. cotnplex metallic ammines. Part VI. cis-Phthalato- cis-homophthalato-and other diethylenediaminecobsltic salts 1982. Dufton Artkzir FeZix the separation of miscible liquids by distillation 1988. Dnnnicliff Horace Barratt and Gerald Snowden Butler ethyl hydrogen sulphate 1384. Dunnill Sydney overvoltage. Part I. A comparison of the methods of determination especially as applied to the mercury cathode 1081. Dutt PaEitra Kmtar E*tcyh Robinson Whitehead and Arthur Wormall, the action of diazo-salts on aromatic sulphonaniides.Pnrt I. 2088. Dutt Sikhibhushan. See Edwin Roy Watson. E. Ewbank (Hiss) Elinor Katharine. See A‘evit Vincent Sidgwick , F. Fairbourne Arthur the o-dimethyl-antliraquinones and their derivatives, 1573. Fairbourne Arthur and Barold Toms, a-monosodium glyceroxide its structure and application 1035. a new synthesis of oxazines 2076. Fargher Robert George arylazogly-oxalinecarboxylic acids 158. Fargher Robert George and liarold King additive compounds of anti-pyrylaminodiacetic acid and its salts with neutrul salts 292. Fargher Robert George and William Henry Perkin gun. m-opianic acid (4 :5 -dimethoxy -0-aldehpdobeneoic acid) 1724. Fargher Ro6ert George and Frank Led Pyman 4-8-methylaminoethylgly-oxaline $34.Farmer Ernest Barold and Christop?m Kelk Ingold the conditions under-lying the formation of unsaturated and cyclic compounds from halogenated open-chain derivatives. Part I1 J. Products derived from halogenated glutsconic acids 2001 2140 INDEX OF' AUTHORS. Field (Mzks) Ellen mitragynine and mitraversine two new alkaloids from species of Mitragyne 887. Findlay Alexander and TViZiMiam Thomas influence of colloids on the rate of reactions involving gases. Part 1. Decomposition of hydroxvl-amine in the presence of colloidal platinum 170. Firth James Brierley some factors governing the sorptive capacity of charcoal ; sorption of ammonia by cocoa-nut charcoal 926. the sorption of hydrogen by amorphous pallatliurn 1120.Firth James Nrierlcy. See also John Driver. Fleck A lexunder. See Tho+nas Wallace. Fletcher (8ir) Lazarus obituary notice Foreter Hartin Onsloz aud FViZliam Bristow Saville studies in the cam-ptiaae series. Part XXXIX. p -Aminophenylaminocarnplior (caniph-oryl-p-phenylenediamine) 789. Friend John Albert Newtoit a colloid theory of the corrosion and passivity of iron and of the oxidation of ferrous salts 932. electrochemical conceptions of valency, 1040. Froelicher Victor and Julius Bcrend Cohen the nitro- and amino-derivatives of m-hydroxybenzoic acid 1425. of 547. G. Garner William Edward and Douglas Norman Jackman catalysis of the niutarotation of dextrose by metals, 1936. Garner William Edward and Kichi-matns Matsuno the explosion of acetylene and nitrogen 1903.Gautier Emile Justin Armand obituary notice of 537. Geake Artlmr. See dlaximilian Nie-renetein. Qibaon David Tcmplelm and Alexander Killen Macbeth the action of alkyl nitrates on piperidine 438. Gibson William Howieson. See Oscar Lisle Brady. Qlaastone 8amw1 physical Chemistry of the oxides of lead. Part I. The solubility of lead monoxide 1689. physical chemistry of the oxides of lead. Part 11. The supposed enan-tiomorphy of lead monoxide 1914. the direct iodometric estimation of lead peroxide 1997. Qlover Thomas. See Gilbert Thomas Goddard Archibald Edwin organo-derivatives of thallium. Part I. Some reactions of thalliiinidialkyl haloids 672. metallic derivatives of nitroplienolic compounds.Part I. Interaction of barium strontium and calcium hydroxides with the mononitro-phenols 1161. organo-derivatives of thallium. Part 11. Interaction of thalliunidialkyl hydroxides with nitrophenols and nitrocresols 1310. Goddard Archibidd EdwiiL. See also (Nm. ) Dorothy Qoddard. Goddard (Mrs.) Dorothy and Archibald h'dwin Goddard metallic derivatives of nitropheiiolic compounds. Fart 11. Soine nitrotolyloxides of metals of Group II. 2044. Qough William Hemy. See Stanley Francis Birch. Graham Hugh and Alexander Kille7A Yacbeth colorations produced by substituted nitroforms 1362. Grant Reginald Lindsay and Frank Lee Pyman the nitro- and amino-dc rivati v es 4 - phen y lgly oxaline , 1893. Green Stanley Joeeph and Thomas Slater Price the chlorovinylchloro-arsines 448.Grifiith Robert Owen and WilLiam James Shutt the decomposition of ozone by light of the visible spectrum, 1948. Gri5th8 Evan Dalton. See Fred Barrow. Grist William Xobinson. See Gilbert l'homm Morgan. Gupta Siraj Mohan an investigation on the influence of negative groups of different character on the reactivity of hydrogen atoms carried by tho same carbon atom. Part I. 298. Morgan. of H. Hamer (Miss) Fyanccs Mary 3 coin-parison of some isomeric isocyanines, 1432. Hammick Dalzicl Llewellyn and John Myhe Mullaly the dimorphism of potassium ethyl sulphate 1802. Harding Leonard the melting points of mixtures of 0- and p-toluenesulph-onyl chlorides 260. the sulphonation of toluene with chlorosulphonic acid 1261 1NDEX OF AUTHORS.2141 Harris John Edmund Guy. See William Hobson Mills, Haworth Ruben! DOW?LS and Arthur Lapworth reduction of emulsified nitro-compounds. Part 11. Some extensions of the method 763. Haworth Walter hTormmn and Edwwn.d Langley Hiret the constitution of the disaccharides. Part V. Cellobiose (cellose) 193. Hedley Thomas Johnson an improved gas conibustion furnace for use in organic analysis 1242. Heilbron lsidor Morris and Johannes Xybrandt Buok the reactivity of doubly-conjugated unsaturated ke-tones. Part I. 4’-Dimethylamino-2-hydroxydistyry 1 ketone 1500. the reactivity of‘ doubly-conjugated unsaturated ketones. Part 11. The action of Iiydroxylamine serni-carbnzide and phenylhydrazine on 4‘-dimethylainino-2-hyd~oxydi-styryl ketone and its niethyl ether, 1515.Heilbron Isidor illorris. See also Edward made9 Oyril Baly. Henderson George Gerald and Joseph Kenneth Marsh contributions to the chemistry of the terpenes. Part XX. The action of hypochlorous acid on pinene 1492. Henry Thomas Anderson and H ~ L ~ I I -phrey Paget chenopodium oil 1714. Henstock Eerbert the bromine com-pounds of phenanthrene. Part I., 55. Iiepworth Harry the action of the Grignard reagent on certain nitric esters 251. the action of the Grignard reagent on certain tervalent organo-iodo-com-pounds 1244. accelerated formation of magnesium alkyl and aryl haloids 1249. Repworth Harry and Henry WiZZiarn Clapham the action of the Grignard reagent on certain organo-sulphur compounds 1188.Hickinbottom Wilfred John. See Gilbert Thomas Morgan. Higeon Geofrey Isherwood the reaction between yersulphates and silver 2048. Hinehelwood Cyril Norman some physico-chemical problems connected with the stability of explosives 721. Hirst Edmund Langley. See Walter Norman Haworth. Hudleston Lawson John and Henry Basaett jun. equilibria of hydrofluo-silicic acid 403. 990-dihydrophenau threne 146 1. Hulton Hewy Francis Everard. See Jzdian Levett Baker. I. Ingold Christopher Kelk the conditions underlying the formation of un-saturated and cyclic compounds froin halogenated open-chain de-rivatives. Part I. Products de-rived from a-halogenated glutaric acids 305. the mechanism underlying the re-actioii between ethyl cyanoacetate and tautomeric substances of the keto-enol type 329.experiments 011 the synthesis of tbe polyacetic acids of methane. Part I. The conditions controlling syn-thesis by the cyanoacetic ester method and the preparation of inetlianetriacetic acid 341. the conditions underlying the forma-tion of unsaturated and cyclic com-pounds from halogenated open-chain derivatives. Part 11. Products de-rived from a-halogenated adipic acids 951. Ingold Christqher Kdk and Edward Arthur Perren experiments on the synthesis of the polyacetic acids of methane. Part 111. Conditions controlling synthesis by the cyano-acetic ester method 1582. experiments on the synthesis of the polyacetic acids of methane. Part 1V. Conditions of formation by the cyanoacetic ester method of stable methanetriacetic esters 1865.Ingold ChAstopher Kelk aud Walter James Powell experiments on the synthesis of the yolyacetic acids of methane. Part TI. Some abnormal condensations of inalonic aud cyano-acetic esters with halogenated me-thanes 1222. experiments on the synthesis of the polyacetic acids of methane. Part V. The preparation of carboxy-methanetriacetic acid 1869. the reversibility of the Michael re-action 1976. Ingold Chwklophcr Kelt and Jocelyn Field Thorpe the chemistry of the glutaconic acids. Part XII. The simultaneous occurrence of 1% and of 1:3-addition to “nascent ” gluta-conic ester 492. Ingold Christopher Kelk. See also finest Harold Farmer. [redale Thomas the r6le of protective colloids in catalysis.Part I. 109 2142 INDEX OF fredale Thomas the soaps as protective colloids for colloidal gold 625. Irvine James Colguhozcn and Jokn Walter fly& Oldham the constitution of polysaccharides. Part 111. The relationship of I-glucosan to d-glucose and to cellulose 1744. J. Jackman Doug2as hTornzan. See William E'dward Qarner. Jaeger Frnns Mawits the action of light of short wave-lengths on some organic acids and their salts 2070. Jenkins WilEiam Job interaction of acetylene and mercuric chloride. Part II. 747. Joner ;k". R. See Gilbert Thornus Morgan. Jonea Leslie Amid. See Gilbert Thomas Morgan. X. Keffier Leon Pierre George some de-rivatives of anthraquinonedi-imide, 1476. Kenner James and W i l f . 2 Victor Stubbings a second form of 6 6'-dinitrodipkenic acid and its conver-sion into new cyclic systems 593.Kenner James and Ernest Witham the influence of nitro-groups on the re-activity of substituents in the benzene nucleus. Part IV. The condensation of ethyl 3- and 5-nitro-2-chlorobenzontes with hgdrazines, 1053. the influence of steric factors on intra-molecular condensation 1452. Kenner James. See also Harold Burton. Kermack Wdlinrn Ogilvy 1VillirCm Henry Perkin jun. and Robert Robin-son harmine and harmaline. Part V. The synthesis of norharman 1602. Kinch Edward obituary notice o f , 2123. King Harold derivatives of sulphur in commercial salvarsan. Parts I. and II. 1107 1415. King HaroEd. See also Robert George Fargher. King Joseph EdgaT.See Abu Mohained Bakr. King (Miss) Ruth production o f pic& acid from the sulphonic acids of phenol 2105. Kipping Frederic StanEey organic derivativee of silicon. Part XXIV. dl-Derivatives of silicoethane 647, AUTHORS. Xipping Preddric Stanley and James Edztiin Sands otganlc derivatives of silicon. Part XXV Srsturated and unsaturated silicohvdrocarbonro, Si,Ph, 830. organic derivatives of silicon. Part XXVI. Piperidine as an analytical reagent 848. Knaggs (iiliss) Isabel BEZie and Richard Henry Vernon organic derivatives of tel1uriu;ii. Part I1 I. Crystallographic anti pharmacological 6omparGon of the a- and 8-dimethyltehronium di-haloids 105. Kon George Amitnizd Robert the forma-tion and stability of spiro-compounds. Part IV.Ketones derived from open-chain and cyclic glutaric acids 810. Kon George Arm,nnd Robert and Arnold Stevenson the formation of derivatives of tetrahydronaphthalene from y-phenyl fatty acids 87. Pon George Armand Robert. See also Stanley Francis Birch. Krishna Xri phenolcoumsrein and resorcinolcouniarein 1420. Krishna Sri and Frank George Po-pe, the condensation of wt-dimethyl-aminophenol with benzaldehyde, 286. Xumar h7at?ik~6mar. See (Sir) Pfc6phldla plien olcitraconein 28 9. C-'landra RQy. L. Laing (Miss) Mary Evelyn. the hydra-tion of the fibres of soap curd. Part 111. Sorption of sodium palmitate, 1669. Lal Jiwan. Lal Miri. Lambourne Herbert. See William Hobson Mills. Lapworth Arthur and (~11~s.) L.ecnwre Kletz Pearson reductiou of emnlsified nitro-compounds.Part I. 8-Phenyl-hyd roxylaniine from nitrobenzene, 765. Lapworth Arthur. See also Robert Downs Raworth. Le Sueur Henry R d e l obituary notice of 2125. Le Sueur Henry Rondel and CyriE Christian Wood the mechanism of the action of fused alkalis. Part 11. The action of fused potassium hydroxide on phenylglyceric acid 1697. Levin (:llliss) Esther. See Fredwick Bauricc Rowe. L a g CyriZ Noman Bug& See Jfauri~ Copirarow. See Bawn Kartar Singh. See Bnuin Karlnr Singh INDEX OF AUTHORS. 2143 Lengstaff George Blundell obituary Losanitch Sima M. note on dithio-notice of 2127. carbazinic acid 763. M. XcBaia Jumeo William and H0rZld7-t Ernest Martin the hydration of the fibres of soap curd. Part I.The degree of hydration determined in experiments on sorption and salting oiit 1369. McBain James William and Cyril Sebastian Salmon the hydration of the fibres of soap curd. Part 11. The dew-point method 1374. Yacbeth Alexander h’illen and David Dodg Pratt the halogen derivatives of nitroform 354. the labile nature of the halogen atoms in substituted nitromethanes, 1356. wagbeth Alexander Xillen. See also David Templeton Gibson and Hzlgh Graham. McClelland Ernest Wilson. See Samuel Smiles. YcCombie Hamilton. See Albert Eric Cashmore. McKenzie Alexander and Fred Barrow, @-a,mino-@-phenylpropiophenone 69. McKenzie Alexander and John Scott Watker Boyle action of magnesium pbenyl haloids on diphenylchloro-acetyl chloride ; constitution of tri-phenylvinyl alcohol 1181.IKcKie (Miss) Phyllis Violet determina-tion of the composition of wixtures of eugenol and isoeugenol benaoates by means of melting points i 7 7 . McKie (Miss) Phyllis Violet. See also Kennedy Joseph Previtd Orton. XaLeod Charles Maxwell; and (ilh.) Gedrude M a d Robinson researches on pseudo-bases. Part 111. Dialkyl-aminomethyl alkyl ethers and aulph-ides 1470. XcYillan Andrew. See Thomas Stewart Pgtterson. Mann Frederick George (Sir) William Jackson Pope and Xichard Henry Vernon the interaction of ethylene and gnlphur monochloride 634. Manning Alexander Bernard the in-fluence of neutral salts on the hydro-lysis of ethyl formate 2079. Marrack (Miss) Muriel Tregarthen. See Tom Sidney Moore. Xsreb Joseph Kenwth.See George Gerdd Henderson. Martin Herbert Ernest. See James William XcBaia. Mason Frederick Alfred B-hydroxy-8-3 4-methylenedioxyphenylethyl-amine and its derivatives 1077. Mat mno Kichimat szb . See TVil Ziam Edward Garner. Haxted Edward Bradford the influence of mercury sulphur arsenic and zinc on the catalytic activity of platinum 225. on the relation between the occlusive power of palladium for hydrogen and its activity far catalytic hydro-genation 1280. Meldrum Andrew Arormnn. See Kup-chand LiEarcm Alimchandani. Hills Ednwnd James obituary notice of 2130. Mills William Wobson Johu Edrnum? G i q Harris and Herbert Lambourne, the Doebner-Miller qninaldine syn-thesis 1294. Mills Jillinm I€obson and Charles Reynolds Nodder the optically active forms of the ketodilactone of benzo-phenon e-2 4 :2’ 4’-te tracarboxylic acid 2094.Mitchell Alec Dwncan studies on hypophosphorous acid. Part III. Its reaction with mercuric chloride 1266. Xoir James the ca,l,cnlation of the colour of “ cyclic coloured sub-stances 1654. Yonier - Williams Gordon Wickham the hydrolysis of cotton cellulose 803. Ildoore Benjamim photosynthetic pro-cesses in the air upon the land and in the sea in relation to the origin and continuance of life on the earth, 1555. Moore Tom Sidney and (Miss) Ida Donbleday some new tricyclic bases, 1170. Moore Tom Sidney (Miss) Muriel Tregarthen Marrack and (Miss) Annie Kathleen Proud the application of Hofmson’s reaction to substituted phthalimides l r S 6 .Morgan Gilbert Thomas and Henry Burgess non-aromatic diazonium salts. Part VI. 3:5-Dimethyliso-oxazole-4-diaaonium saits and their azo-derivatives 697. non-aromatic diazonium salts. Part VII. The diazo-reaction in the isooxazole series 1546. Morgan Gilbert Thomas and William Arthur Percival Challenor [with F. R. Jones] o-chlorodinitrotoluenes. Part 111. Bases derived from 2-chloro-4 5 - dini trotoluene 15 3 7 2144 INDEX OF AUTHORS. Morgan Gilbert Thomas and Harry Dugald Keith Drew researches on residual affinity and co-ordination. Part 111. Reactions of selenium and tellurium acetylacetones 610. researches on residual affinity and co-ordination. Part V. Gallium ncetylacetone and its analogues, 1058. Xorgan Gilbert Thomas and Thomas Glover o-chlorodinitrotoluenes.Part IV. 2-Cliloro-3:4-dinitrotoluene 1700. Morgan Gilbert Thomas and William Robinson Grist arylsulphonylnaph-thylenediamines and their snlphonic acids 602. Morgan Gilbert Thomas and Wi7fred John Hickinbottom studies in the It-butyl series. Part I. Aryl n-propyI ketones 1879. Morgan Gilbert Thomas and Leslie Amiel Jones o-chlorodinitrotoluenes. Part II. 187. Morgan Gilbert Thomas and J. D. Main Smith researches on residual affinity and co-ordination. Part IV. The constitution of simple and com-plex cobaltic qninoneoxime lakes, 704, researches on residual affinity and co-ordination. Part VI. Seleno-dithionic acid and its metallic salts, 1066. Morgan Gilbert Thomas and Dudley Cloete Vining dihydroxynaphth-aldehydes 177.dinaphtha-l:7:lf:7'-diquinone 1707. Morgan Gilbert Thomas and (Miss) Dorothy Webster diazo-derivatives of 4'-arnino-l-phenyl-5-methylbenzothi-azole (dehydrothio-p-toluidine) 1070. Morgan John David and Richard Vernon Wheeler phenomena of the ignition of gaseous mixtures by in-duction coil sparks 239. Xullaly John Mylne. See Dakiel LleweElyn Hammick. N. Xagel David Henry obituary notice of, Naik Kuverji Gosai the formation and properties ofdithio-ketones (IL,C:S:S) and dithio-ethers (R,S:S). Parts I. and II. 3i9 1231. interaction of sulphur monochloride and organic acid amides 1166. Newbery Edgar chlorine overvoltages, 477. 551. Nierenstein Mamhzdian the constitu-tion of catechin. Part 111. Synthesis of acacatechin 164.Nierens tein Maximi Zian Char les Wi I -liam Bpiers and Arthur Oeake gallo-tannin. Part XII. 275. Nodder Charles Reynolds. See William Hobson Mills. Norris IVoodford Stanley Gowan Pluck-nette and Jocelyn Field Thorpe the formation and stability of spiro-com-pounds. Part V. Derivatives of cyclo-hexanespirocyclohexane and of cyclo-pentanespirocyclohcxane 11 99. 0. O'Connor Edmund Art7~ur the binary system aniline-acetic acid 400. Odling Rl'illiam obituary notice of, 553. Oldham John Walter Hyde. See James Colphoun Irvine. Orton Kenned!j Joseph Prcvitt? and (Miss) Phyllis Violet McKie preparation of chloropicrin from picric acid and trinitrotolueoes 29. P. Packer John and h n Willium War%, cupritartrates 1348. Paget Humphrey.See Thomas Ander-son Henry. Patterson Thomas Stewart and Andrew BdcYillan the action of ammonia on acetone 269. Pearman Sydney Albert derivatives of m-xylem 717. Pearson (Mrs. ) Leonore Kletx. See Arthur Lapworth. Perkin William Eenry jun. the action of sodium on phenyl acetate 1284. Perkin William Henry jun. and Sydney Glenn Preston. Plant deriv-atives of tetrahydrocarbazole 1825. Perkin William Henry jz~n. and Eric Robinson studies on the configuration of ad-dibroniodibasic acids. Part J. The dibromoadipic acids ; synthesis and resolution of trans-cyclopentane-1:2:3- tricarboxylic acid 1392. Perkin William Henry jun. and Harold Archibald Scarborough reso-lution of dl-trans-cyclopentane-1 3-dicarboxylic acid 1400. Perkin William HenTy jun.and Alan Francis Titley epicamphor. Part II., 1089. Perkin WzTliam Henry jm. and Stanley Horwood Tucker the oxida-tion of carbazole 216 INDEX OF AUTHORS. 2145 Perkin William Henry jun. See also Robert George Fargher and William Ogilvy Kermack. Perman Edgar Philip. See (Miss) Jane Bonnell. Perren Edward Arthzcr. See Chris-topher Kelk Ingold. Pickering Spencer Percival Umfreuille, obituary notice of 564. Pickles Aluyn negative adsorption of alkali haloids by wood charcoal 1278. Pike TVilZiam Herbert obituary notice Plant Xgdney Glenn Preston. See William Henry Perkin jun. Pope Frank George. Pope (Sir) William Jackson and James Leonard Brierley Smith the inter-action of sulphur monochloride and substituted ethylenes 396. Pope (Sir) William Jackson.See also Frederick George Mann. Porter (Miss) Mary Winearls crystallo-graphic descriptions of some pyridine and picoline derivatives 1769. Powell Alan Ricktrd. See Walter Raymond Schoeller. Powell Walter Jams. See Christopher Kelk Ingold. Pratt David Doig. See Alexander Xillen Xacbeth. Price Thontas Slater. See Stanley Joseph Green. Proud (Miss) Annie Kathleen. See Tom Sidney Moore. Pyman Frank Lee. See Bobert George Fargher and Xeginald Lindsay Orant. of 539. See Xri Krishna. R. Raa Madyar Copal. See John Lionel Simonsen. Ray Francis Earl. See Fyederick Daniel Chattaway. Ray Jiianendu Nath syntheses in the thianthren series 1959. Ray (Sir) Praphulla Chandra and Kalikumar Kumar the molecular conductivity of aome sulphonium compounds in acetone 1643.Ray Priyadaranjan and Pzcli.rt Vihari Sarkar compounds of hexamethylene-tetramine with complex metallic salts and acids 390. Bead John and (Miss) Alberta Catherine Pritchard Andrews studies of halogenohgdrins and related deriv-atives in the cinnamic acid series. Part I. 1774. Read John and Henry George Smith, piperitone. Part I. The occurrence, isolation and characterisation of piperitone 779. Reilly (Miss) Amy Ada Beatrice. See John Norman Collie. Renouf (Miss) Nora. See Arthzcr TVil7iam Crossley. Report of the Council 513. Report of the International Committee on Physico-chemical Symbols 502. Reynolds William C'olebrook on iuter-facial tension. Par1 I. The statical measurement of interfacial tension in absolute units 460.on interfacial tension. Part 11. The relation between interfacial and surface tension in sundry organic solvents in contact with aqueous solutions 466. Rivett Albert Cherbury David. See Frderick William Jefrey Clendinnen. Robertson (Sir) Robert some properties of explosives 1. Robinson Eric. See William Henry Perkin jun. Robinson (Mrs.) Gertrude Maud. See Charles Maxwell XcLeod. Robinson Robert. See William Ogilvy Kermack. Rowe Frederick Mawice and (Miss) Esther Levin studies in the dihydro-naphthalene series. Part 11. The ar-dihydro-a-naphthols and their derivatives 2021. Rubie Howard Ernest. See Nevi1 Vincent Sidgwick. Ruffle John obituary notice of 541. 13. Salmon Cyril Sebastian. See James William McBain.Sands James Edwin. See Prederic &anley Kipping. Sarkar Putin Vihari. See Priyada-ranjan My. Saville Wdlianz Bristozu. See Martin Onslow Forster. Scarborongh Harold Archibald. See Albert Eric Cashmore and William Henry Perkin jun. Schoeller Walter Raymond and Alan Richard Powell investigations into the analytical chemistry of tantalum, columbium and theii mineral associ-ates. I. The use of tartaric acid in the analysis of natural tantalo-columbates. 11. The separation of zirconium from tantalum and from columbium 1927 2146 lNDEX OF AUTHORS. Iaott John Richard and Jztlizcs Bereircl Cohen on some carbamido-acids and their hydsntoins 664. Shields John obituary notice of 569. Shimomwa Akiru and Julius Berend Cohen physical and physiological properties of aome hydrogenated quinoline compounds 740.8 new method for the resolution of asymmetric compounds 1816. Short Wallace Frank a new method for the preparation of a-acylphenyl-hydrazines 1445. Sidgwick Nevil Vincent and JVilfrid Major Aldous influence of position on the solubility and volatility of tlie mono- and di-nitrophenols 1001, Sidgwick Nevil Vincent. and (Miss) EZinor Katharine Ewbank the stability of tautomeric form-aldehydephenylhydrazones 486. the influence of position on the solubilities of the substituted benzoic acids 979. Sidgwick hTevil Vincent and Howard Ernest Rubie the solubility and volatility of the chloro- and nitro-anilines and of their acetyl deriv-atives 1013. Silberrad Oswald researches on sulphuryl chloride.Part I. In-fluence of catalysts; a convenient method of chlorinating benzene, 2029. Silver Leonard. See William Arthur Bone. Simmonds Charles obituary notice of, 542. Simmone Thontas Arthur. See Henrg Bassett jun. Sirnoneen John Lionel the essential oil from Andropogon JwaranczLsa Jones, and the constitution of piperitone, 1644. Sirnoneen John Lionel and Madyar Gopal Rau synthesis of 1:6-dihydroxy-2-methylanthraquinone, 1339. Singh Bawa Kartar and J i r i Lal, studies in substituted quaternary azonium compounds contairiirig an asymmetric nitrogen atom. Part IV. Additive compounds of thiooarbamide with azonium iodides 210. Singh Bawu Kartar Mahan Bingh, and Jiwan Lal stiidies on the de-pendence of optical rotatory power on chemical constitution.Part IV. Aryl derivatives af bisiminocamphor, 1971. Singh Muhan. See Bawa Xarlar Singh. Slator Arthur yeast craps and the factnrs which determine them 115. Smart Bertram James obituary notice of 544. Smiles 8nrnwl and Ernest Wilson McClelland derivatives of 3-oxy(l)-thionaphtherr 1810. Smiles Sn??az&eZ and ( Ariss) JeJsie Stewart m-dithiobenzoic acid 1792. Smith Henry George. See John Read. Smith J. D. Main. See Gilbert Thomas Smith James Leonard BrierZey. See Smith Robert Christie. See Robert Spiers Churh William. See Haxi-Stedmaa Edgar a new degradation Stevenson Arnold. See George Amzcwd Stewart (Miss) Jeesie. See SamueE Stnbbings WiEfrid Victor. See Jameo Sugden Samuel on reduction by metals in acid solutions.Part I, The reduction of acid ferric Yulphate solutions by zinc and magnesium, 233. the determination of surface tension from the rise in capillary tubes, 1483. Morgan. (Siy) W-illiam Jackaon Pope. Wright. m ilian Nierens tein. product of physostigmine 891. Bobert Kon. Smiles. Kenner. T. Thom88 Richard and Edward Thomas Williams the catalytic oxidation of ferrous salts in acid solutions 749. Thomae William inorganic complex salts. Part I. Potassium ferrioxalate and potaesium cobaltimalonate 1140. Thomas William. See also AEexander Findlay. Thorne Percy Cyril Lesley the solubility of ethyl ether in solutions of sodium chloride 262. Thorpe Jocelyn Field. See Chrietopher Kelk Ingold and Woodford Stanley Gowan Plucknedte Norris.Titley Akan Francis. See William Henry Perkin jun. Tizard Henry Thomud and Alfrcd Reginald Boeree the volumetric esti-mation of mixtures of acids and of bases and of polybasic acids or bases, 132. Tome Barold. See Arthur Pairboame. Triffitt (Miss) Phyllis Mary. See EolZand Crompton INDEX OF AUTHORS. 2147 Tuaker Stanley Horwood. See William Turner Eustace Ebenecer. See Ceorge Henry Perkin jzm. Joseph Burrows. V. Vernon Richard Henry organic deriva-tives of tellurium. Part IV. Action of ammonia and the alkalis upon a-dimethyltelluronium di-iodi!e 687. obituary notice of 2132. Vernon Richard Henry. See also (Miss) Isabel Ellie Knaggs and Frederick George Mann. Vining Dudley Cloete. See Gilbert Thomas Morgan.W. Walker Eric Everurd surface tensions of salts of the fatty acids and their mixtures 1521. Wallace Thomas and Alexander Fleck, some properties of fused sodium hydr-oxide 1839. Ward Charles Frederick the use of aluminium chloride and ferric chloride in the preparation of phenolphthalein, 850. Ward Charles Frederick. See also Samuel Coffey. Wark Inn William. See John Packer. Watson Edwin Roy and Sikhibhushnn Dutt dyes derived from phenanthra-quinone 1211. Webster (Mws) Dorothy. See Oilbert Thomas Morgan. West Ealyh Winton. See John Valen-tine Backes. Wheeler Richayd Verno,i See Joh.lt David Morgan. Whincop (Miss) Edith Muriel. See Ceorge iCPacdonald Bennett. Whinyates Leonard. See Fyederick William Atack. Whitehead Hugh Robinson. See Pavitra Kumar Dutt. Whiteley (Miss) Martha A.rtnie. See John VaZentine Backes. Williams Bdward Thomas. See Richard Thomas. Wilson Leonard Philip obitnary notice of 571. Witham Ernest. See James Kenner. Wood C y d Christian. See Benry Rondel Le Sueur. Wormall Arthur. See Pavitra Kwwr Dutt. Wren Henry and Edward Wxight, studies in the resolution of racemic acids by optically active alcohols. Part 11. The resolution of atrolactinic and a-hydroxy-8-phenylpropionic acids by I-menthol '198. Wright Edward. See Eenry Wren. Wright Robert and Robert Christie Smith the effect of temperature on platinum black and other finely-divided metals 1683. Y. Yeoman Erneat Wickham trithiocarb. onates and perthiocarbonates 38

ISSN:0368-1645    

DOI:10.1039/CT9211902137

出版商:RSC    

年代:1921

数据来源: RSC

摘要:

INDEX OF SUBJECTS. TRANSACTIONS. 1921. Single organic compounds of knowii empirical fprnlnla mill be found in the Formula Index p. 2155. A. Awatachin synthesis of (NIEREN-Icetylacetones metallic (MORGAN and DREW) 1058. Acids estimation of volumetrically (TIZARD and BOEREE) 132. fatty surface tensions of salts of and their mixtures (WALKER) 1521. organic and their salts action of light on (JAEGER) 2070. a -8cylphenylhydrazines ( SH o RT) I 4 4 5. Adaur@ion by charcoal ( BAKIL and XINO) 454 ; (FIRTH) 926 ; (DRIVER negative by wood charcoal (PICKLES), Aanity residual and co-ordination (MORGAN and DREW) 610 1058; (MORGAN and SMITH) 704 1066. Alkali haloids negative adsorption of, by charcoal from aqueous solu-tions (PICKLES) 1279. additive compounds of antipyryl-aminodiacetic acid and its salts with (FARGHER and KING) 292.Alkalis fused mechanism of the action of (LE SUETJR and WOOD) 1697. Alkaline earth haloids additive corn-pounds of antipyrylaminodiacetic acid and its salts with (FARGHER and KING) 292. Alkaloids salts of with hexabromo-stearic acid (COFFEY) 1309. Alkyl nitrates action of piperidine with (GIBSON and MACBETH) 438. Aluminium chloride use of in the pre-paration of phenolphthalein (WARD), 850. Amides acid organic action of sulphur monochlorido on (NAIK) 1166. Ammines complex metallic (DUFF) 385, 1982. Ammonia adsorption of by charcoal action of on acetone (PATTERSON and STEIN) 164. and FIRTH) 1126. 1278. (FIRTH) 926. MCMILLAN) 269. Ammonium tri- and per-thiocarbonate~ (YEOMAN) 61.chloride equilibrium of manganous chloride water and (CLENDINNEN and RIVET~) 1329. selenoditliionate (MORGAN and SMITH), 1068. iron alum colour of (BONNELL and PERMAN) 1994. Amylase of rye (RAKER and HULTON), Analysis organic gas combustion furnace for ( HEDLEY) 1242. volumetric of acids and bases (TIZARI) and BOERICE) 132. Adropogon Jwnmncusa essential oil from (SIMONSEN) 1644. Annual General Meeting 513. Anthracene series studies in the (BAR-NETT and COOK) 901. Antimony triiodide .action of phenyl-dimethylarsine with (BURROWS and TGI~NER) 1449. Arsenio triiodide action of phenyldi-methylarsine with (BURROWS and TURNER) 1449. Araenic organic compounds (~Unaows optically active preparation of (BUR-Arylazoglyoxalinecarboxylic acids Asym’metric compounds resolution of Atmospheric air ignition of mix-tures of ethylene and (CHAPMAN), 1677.ignition of mixtures of methane and (MORGAN and WHEELER) 241. Atomic weights and mass-spectra (As-Atrolactinic acid C,H,,O,. Azine scarlets structure and colour of (COHEN and CRABL’REE) 2055. Azonium compounds substituted qua-ternary containing an asymmetric nitrogen atom (SINGH and LAL), 210. 805. and TURNER) 1448. ROWS and TURNER) 426. (FAltQHER) 1.58. (SHIMOMURA and COHEN) 1816. TON) 677 INDEX OF SUBJECTS. 21 49 B. Balanoe sheets of the Chemical Sociat-y and of the Research Fund. See Annual General Meeting 513. Barium tri- and pcr-thiocarbonrttes ( YEO-selenodithionate (MORGAN and Sar r m ) , Baser tricyclic (I\~OOXE and DOUBLE-estimation of voliimetrically (TIZARD $-Bases researches on (MCLEOD and Benrene nucleus influence of the chlor-ine atom and the methyl and sulplionyl chloride groups on sub-stitution in the (DAVIES) 853, 876.influence of nitro-groups on the reactivity of substituents in the (BuaTox and KENNER) 1047; (KENNER and WITHAM) 1063. migration of dkyl groups in the (COPISAROW) 1806. migration of halogen atoms iu the (COPISAROW) 442. Bemoio acids substituted influence of position on the solubility of (SIDGWICK and EWBANK) 979. Bbmuth triiodide action of phenyl-diiiretbylarsine with (BURROWS and TURNER) 1449. Bismuth organio compounds :-Bismnthines tertiary aromatic halo-gem derivatives action of with magnesium and mercury organic compounds ( CIIALLENQER and ALL-PRESS) 913.Ic-Butyl series studies in the (MORGAN MAN) 48. 1068. DAY) 1170. aird BOEEEE) 132. hBIXSON) 1470. and HICKINBOTTOM) 1879. C. Cmsiam selenodithionate (MORGAN and SMITE) 1068. Caloium tri- and per. thiocarbonates (YEOMAN) 47. Camphane serie~ studies in the (FOIMTER and SAVILLE) 789. Carbaddo-wide and thoir hydantoins (SCOTT and COHEN) 664. Carbarole CI2H N. Carbohydrates pkotospthcsis of ( BUY, HRICBRON and BARKER) 1086. Caronimide C7HB02N. Catalysir function of protective colloids in (IIUCDALE) 109. Catalwtm influence of on the chlorina-tion of benzene (SILBERRAD) 2029. Catechin C15H1,0e. Cathoder mercury overvoltage at ( DUNN I LL) 1081. Cellobiow C12HBOll.Cellose. See Cellobiose. Cellulose cotton hydrolysis of ( MONIEK-WILLIAMS) 803. Charcoal animal adsorption of wshr and alcohol by (DRIVER and FIRTH) 1126. cocoa-nut adsorption of ammonia by (FIRTH) 926. wood adsorption of benzene by alone, and from iodine solution (BAKB and KING) 454. negative adsorption of alkali haloids by (PICKLES) 1278. Chemioal constitution and optioal rota-tion (€3. K. and M. SINGH and LAL) 1971. influence of on reactivity (GUPTA), 298. reactions influence of the solvent on the temperature coefficient of (Cox), 142. Chenopodinm oil constituents of (HENRY and PAGET) 1714. Chlorine overvoltage during liberation of (NEWBERY) 477. pl~otochemical reaction of hydrogen with (BALY and BARKER) 653. Choline C,Hl,O.$T.Coal determination of the volatile matter from (BONE and SILVER) 1146. Cobalt baser (cubaltammilus) complex (DUFF) 385 1982. Cobalt lakes with qninoneoximea con-stitution of (MORUAN and SMITH), 704. Colloids influence of on the velocity of reactions involving am8 (FIND-LAY and THONAS) do. protective function of in catalpie (IREDALE) 109. Colloidal solutions interfacial and surface tensions of (REYXOLDB) 471. Colour calculation of of coloured cyclic compounds (MoIR) 1654. Colonring matters cobaltic quinone-oxime (MORGAN and SMITH) 704. vim-Compounds formation and stability of (ICON) 810 ; (NORRIS and THORPE), 1199; (BIRCH COUGH and KoN), 1315. Co-ordination and residual affinity (MORGAN and DREW) 610 1068; MORGAN and $MITE) 704,1066.Copper action of nitric acid on (BAG-methylation of (DENHAM) 77. soaps as (IREDALE) 626. an6 valency ( BRIGGS) 1876. BTER) 82 2150 INDEX OF SUBJECTS. Copper action of fused sodium hydr-oxide on (WALLACE and FLECK), 1849. Copper organic compounds :-Cupritartrates (PACKER arid WAKK), GoCyanines isomeric (HAJIER) 1432. Cyclic compounds formation of from halogenated open-chain derivatives (INGOLD) 305 951 ; (FARMER and INGOLD) 2001. coloured calculation of the colour of (Mom) 1634. 1348. D. Diaso-salts action of on aromatic sulphonamides (DUTT WHITEHEAD, and WORMALL) 2088. Diazonium salts non-aromatic (MORGAN and BURGESS) 697 1546. Diethylaminomethyl alkyl ethers and snlphides preparation of (MCLEOD and ROBINSON) 1472. Dihpdronaphthalene series studies in the (ROWE and LEVIN) 2021.Dimethylpyrone C7H,0,. Disaccharides constitution of (HA-WORTH and IirRs'r) 193. Distillation separation of miscible liquids by (DUFTON) 1988. m-Dithiobenzoic acid C,,H,,O,S,. E. Xllagic acid C1,H60, Emulsions studies in (BHATNAGAR)~ 61 1760. Enzymes :-Amylase. Epicamphor C,,H,,O. Equilibria chemical influence of salts on in solution (BI:OPTBTED) 574. Eserine C,,H,,O,N . Es ters as-unuatn rated condema tion of, with sodio-malonic esters (ISGOLD and POWELL) 1976. Ethers dithio- formfition and properties of (NAIK) 379 1231. Ethyl esters velocity of saponification of (CASHMOSS MCCOMRIB and SCAn-BOROUGH) 970. Eucalyptus oil cbstituents of (READ and SMITH) 779. Eugenol Cl,H,,O,.Explosives properties of ( ROBEIWSON) 1. thermal decomposition of (HINSHI~L-WOOIJ) 721. F. Ferric and Ferrous salts. See under Iron. Flame propagation of in mixtures of ethylene a1141 air (CHAPMAN) 1677. Fluorene Cl~~Tlo. Fluorine :-Hydroflnosilicic acid equilibria of ( HUDLESTON and BAssETT) 403. Formaldehpdephenylhydrazones snb-stituted tautomeric stability of (SIDG-WICK and EWBANK) 486. Friedel-Crafts' reaction (COPISAROW), 442 1806. Furnace gas combustion for use in organic analysis (HEDLEY) 1242. 0. Gallic acid derivatives (ALIMCHANDANI and MELDRUBZ) 201. Gallium organic compounds (MORGAN arid DREW) 1058. Gallo tannin ( NIENEKSTEIN S PI ICKS and GICAKE) 275. Gaaes ignition of mixtures of (MORQAX and WHEELER) 239 ; (CEIAPMAX), 1677.Gas reactions influence of colloids on the kinetics of (FINDLAY and THOMAS), 1 70. Glucinum (bcryZZium) sulpli:ite solii-bility of in water and sulphuric acid (BKITTON) 1967. equilibrium in the system potass-ium sulphate wnter and (BRIT-TON and ALIXAND) 1463. 8-Glucosan C6H,,0,. Glutaconic acids chemistry of ( IKGOLD and THOKPE) 492. Gold colloidnl soaps RS protective colloids for ( IREDALE) 625. Grignard reagents action of on nitric esters (HEPWORTH) 251. action of on organic iodine compounds (HIEPWORTH) 1244. action of on organic sulphur com-pounds (HEPWORTH and C L A I x o f ) , 1188. H. Harmaline C,:;€I,,OSz. Harmine C,2H,,N,. Hofmann's reaction application of to subs ti t u teti ph thalimid cs (Moo RE, MAILRACK and PROUD) 1786.Hugo Miiller Lecture (MOORE) 1555. Hydrofluosilicic acid. See under Hydrogen photochemical reaction of chlorine with ( BALY and BARKER), 653. absorption of by palladium (FIRTH), 1120 ; (MAXTED) 1280. Fluorine INDEX OF SUBJECTS. 2151 Hydrogen atoms influence of negative groups on the reactivity of (GUPTA), Hydrexy-aaids esters condensation of ethyl sodiocyanoacetatewith ( IKGOLD), 336. Rydroxylamine decomposition of in presence of colloidal platinum (FIND-LAY and THOMAS) 170. Hjpophosphorous acid. See under Phosphorus. I. Isnition of mixtures of gases (MORGAN of mixtures of ethylene and air Indium organic compounds (MORGAN and DREW) 1062. Interfacial tension (REYNOLDS) 460, 466. Intramolecular condensation influence of steric factors on (KENNER and WITHAM) 1452.Iodine organic compounds new type of action of Grignard reagents on Iron corrosion and passivity of action of fused sodium hydroxide on ammonium alum colour of (BONNELL Ferric chloride use of in the pre-paration of phenolphthalein (WARD) 850. hydroxide adsorption of thorium-B and -C by (CRANSTON and BURNETT) 2036. sulphate reduction of acid solu-tions of by magnesium and zinc (SUGDEN) 233. Ferrous salts theory of the oxidation of (FRIEND) 932. catalytic oxidation of in acid solution (THOMAS and WIL-LIAMS) 749. 298. and WHEELER) 239. (CHAPMAN) 1677. (COLLIE and REILLY) 1550. (HEPWOHTH) 1244. (FRIEND) 932. (WALLACE and FLECK) 18.12. and PERMAN) 1994. K. Ketones derived from glutamic acids (KoN) 810.unsaturated reactivity of (HEILBRON and BUCK) 1500 1515. Ketones dithio- formation and pro-perties of (NAIK) 379 1231. L. Lead peroxide estimation of iodo-metrically (GLASSTONE) 1997. Lesd oxides physical chemistry of (GLASSTONE) 1689 1014. Lectures delivered before the Chemical Society (ROBERTSON) 1 ; (ASTON), 677 ; (?TOORE) 1655. Life origin and continuance of on the earth (MOORE) 1565. Linolenic acid C,,,H,,O,. Linolic acid C18H,,0q Linseed oil composition of (COFFEY), oxidation of (COFFEY) 1152. Liquids interfacial and surface tensions miscible separation of by distillation Lithium selenodithionate (bfoRGAN and SMITH)^ 1067. 1413. of (REYNOLDS) 466. (DUPTON) 1988. M. Maggesium reduction of acid solutions of ferric sulphate by (SUGDEN), 233.tri- and per-thiocarbonates (YEOMAN), 5 0. Magnesium organic compounds action of with halogen derivatives of tertiary aromatic bismuthinea (CHALLENGER and ALLPRESS) 913. alkyl and aryl haloids catalysis in the formation of ( HEPWORTR), 1249. Malonyl derivativer halogenated melt-ing points of and their quantitative reduction by hydriodic acid (BACKES, WEST and WHITELEY) 359. Manganous chloride equilibrium of ammoniiim chloride water and (CLENDINNEN and RIVETT) 1329. Mercuric chloride action of acetylene action of hypophosphorous acid Mercury organic compounds action of, with halogen derivatives of tertiary aromatic bismuthines (CHALLENGER and ALLPRESS) 913. Mercury cathode. See Cathode.Metallic salts complex (THOMAS) 1140. compounds of hexamethylene-tetramine with (RAY and SARKAR) 390. Metals reduction by in acid solutions (SUGDEN) 233. finely-divided effect of temperature on (WRIGHT and SMITH) 1683. heated action of sodium hydroxide with (WALLACE and FLECK) 1841. Manganese :-Mercury :-with (JENKINS) 747. with (MITCHELL) 1266 2152 INDEX OF SUBJECTS. Methylene group reactivity of the Michael reaction reversibiliiy of the Mitragyne alkaloids from species of Mitragynine U,,H,lO,N. Mitraversine C,,H,O,N (?). Molecular conductivity of sulphonium compounds in acetone (RAY and KUMAR) 1643. (GUPTA) 298. (INGOLD and POWELL) 1976. (FIELD) 887. IT. Nickel action of fused sodium hydroxide on (WALLACE and I'LECK) 1847.Nitric acid. See under Nitrogen. Nitro-compounds emulsified reduction of (LAPWORTH and PEARSON) 765 ; (HAWORTH and LAPWORTH) 768. Nitrogen explosion of acetylene and (GARNER and MATSUNO) 1903. Nitric acid action of on cqpper (BAGSTEK) 82. esters action of Grignard reagents on (HEPWORTH) 251, Nitroprussic acid C,H,ON,Fe. Nitroprussides constitution of (BUR-ROWS and TURNER) 1450. Nitroao-compounds condensation of p -nitrobenzyl chloride with (BARROW and QRIFFITHS) 212. Norharman CllH,N,. Norharmol C,lH,ON,. 0. Obituary notices :-Sir William de Wiveleslie Abney 529. Henry Bassett 532. Albert Edward Bellars 2120. Edward John Bevan 2121. Bertram Blount 545. Alexander Wynter Blyth 545. John Cannell Cain 633. Sir Lazarus Fletcher 547.Armand Gautier 537. Edward Kinch 2123. Henry Rondel Le Sueur 2125. George Blundell Longstaff 2127. Edmund James Mills 2130. David Henry Nagel 551. William Odling 553. Spencer Percival Umfreville Pickering, William Herbert Pike 539. John Ruffle 541. John Shields 569. Charles Simmonds 542. Bertram James Smart 544. Richard Henry Vernon 2132. Leonard Philip Wilson 571. 564. Oils drying oxidation of (COPFEY) 1152, 1408. Optical rotation and chemical consti-tution (B. K. andM. SINGH and LAL), 1971. Overvoltage (NEWBERY) 477 ; (DUN-NILL) 1081.. Oxazines synthesis of (PAIRBOURNE and TONS) 2076. Oximes isomerism of (ATACIC) 1175 ; (ATACE; and WHINYATES) 1184. N-Oximino-ethers formation of (BAR-ROIV and GBIF'FITHS) 212. 3-0xy( l)thionaphtheu C&,OS.Ozone decomposition of by light (GRIFFITII and SHUTT) 1948. P. Palladium absorption of hydrogen by (FIRTH) 1120. relation between the occlusion of hydrogen by and its catalytic activity (MAXTED) 1280. Palmitic acid C,6H,202. Persulphates. See under Sulphur. Phenanthraquinone colouring matters (WATSON and DLTTT) 1211. Phenols nitro- metallic derivatives of (GODDAI~D) 1161; (D. and A. E. GODDARD) 2044. Phenolcitraconein Cl7HL4OP. Phenolcoumarein C,1H2006. Phenolphthalein C20H140,. Phenolsulphonic acida preparation of 5-Phenylacridine ClsH1,N. Phenylopiazone Cl6H1,O3NB. Phosphorus triiodide action of phenyl-dimethylarsine with (BURROWS and TURNER) 1449. Hypophosphorous acid studies on (MITCHELL) 1266. Photocatalysis (BALY HEILBRON and BARKER) 1025.Photochemical reactions with organic acids and their salts (JAEGER), 2070. . Photosynthesis in relation to the origin and continuance of life on the earth (MOORE) 1555. Phthalimides substituted application of Hofmann's reaction t o (MOORE, MARRACK and PROUD) 1786. Physico-chemicalsymbols International, 502. Physostigmine. See Eserine. Picoline derivatives crystallography of (PORTER) 1769. Piperidine C,Hl,N. Piperitone C,H1,O. picric acid from (KING) 2105 INDEX OF SUBJECTS. 2153 Platinum influence of arsenic mercury, sulphur and zinc ou the catalytic activity of (MAXTED) 225. Platinum-black effect of temperature on (WRIGHT and SMITH) 1683. Polysaccharidss constitution of (IRVINE Potassium tri- and per-thiocnrbonates (YEOMAN) 46.hydroxide fused action of on phenylglyceric acid (LE SUEUR and aulphate equilibrium in the system, glucinum sulphate water and ( HRITTON and ALLMAND) 1463. Pyridine C,H,N. Pyridine derivatives crystallography of (PORTER) 1769. and OLDHAM) 1744. WOOD) 1697. Q. Quinaldine C1,H,N. Quinine Ca,H,,O,N,. Quinoline compounds hydrogenated, physical and physiological properties of (SHIMOMURA and OOHEN) 740. El. Itacemic acids resolution of by means of optically active alcohols (WREN and WRIGHT) 798. Radiation hypothesie applied to chemical reactions (Cox) 142. Reactivity influence of constitution on (GUYTA) 298. Rubidium selenodithionate (MORGAN sulphites (MORGAN and SMITH) 1069. Rye amylase of (BAKER and HULTON), 805.and SMITH) 1068. S. Salvarsan commercial sulphur deriv-atives i n (KIKG) 1107 1415. Selenodithionic acid and its metallic salts (MORGAN and SMITH) 1066. Silicon organic compounds (KIPPING), 647 ; (KIPPING and SANDS) 830 848. Silver action of solutions of per-sulphates on (HIGSON) 2048. Soap curd hydration of the fibres of (MCBAIN and MARTIN) 1369; (MCBAIN and SALMON) 1374 ; (LAING) 1669. solutions interfacial and surface tensions of (REYNOLDS) 473. Soaps use of as protective colloids for colloidal gold (IREDALE) 625. Sodium action of 011 phenyl acetate ( I’ERKIN) 1284. CXIX. Sodium hi- and per-thiocarbonates chloride solubility of ethyl ether in hydroxide fused properties of (WAL-selenodithionate tetrahydrate (MOR-fiolubility influence of position in substitution on (SIDGWICK and Ew-BANK) 979 ; (SIDGWICK and ALDOUS), 1001 ; (SIDGWICK and RUBIE) 1013.Solutions influence of salts on chemical equilibria in ( BKONSTED) 574. Solvents mixed velocity of reaction in (CASHMORE MCCOMBLE and SCAR-BOROUGH) 910. Spectra mass and atomic weights (ASTON) 677. 8tannic chloride. See under Tin. Stearic acid 01,H,,Oa. Strontium tri- and pcr-thiocnrbonates (YEOMAN) 49. Strychnine C,,Ha,O,N,. Sulphonamides aroiimtic action of diazo-salts on (DCTT WHITEBEAD, and WORMALL) 2088. Sulpbonium compounds molecular con-ductivity of in acetone (RAY and KUNAR) 1643. Sulphur monochloride action of on organic acid aniides (NAIK) 1166. action of on ethylene (MANN POPE, and VERNON) 634.action of on substituted ethylenes (POPE and SMITH) 396. chlorides action of ou substituted ethylenes (COPFEY) 94. Sulphuryl chloride chlorination of benzene with (SILBERRAD) 2029. Pereulphates action of solutions of, on metallic silver (HIGSON) 2048. Sulphur organic compounds action of Grignard reagents on (HEPWORTII and CLAPHAM) 1188. Sulphuryl chloride. See under Sulphur. 8 urface tension determination of from of saturated liquids (REYNOLDS) 467. of salts of the fatty acids (WALKER), (YEOMAN) 40. solutions of (THORNE) 262. LACE and FLECK) 1839. GAN and SMITH) 1067. capillary rise (SUGDEN) 1483. 1521. T. Tantalum :-Tantalocolumbatee analysis of (SCHOELLEK and POWELL) 1927. Terpenes chemistry of ( HENDERSON and MARSH) 1492.Tellurium organio compounds ( KNAGGS and VERNON) 105 ; (VERNON) 687. Temperatare-coefficients of chemical re-actions (Cox) 142. 4 2154 INDEX OF SUBJECTS. Te trshydrocarbszole C, H Is N. Thallium organic compounds (GOD-DARD) 672 1312. Thianthren series syntheses in the (RAY) 1959. Thorium-R and -12 adsorption of by ferric hydroxide (CRANSTON and BURSETT) 2036. Tin :-Stannic chloride action of pheuyl-dimethylarsine with (BURROWS a i d TURNER) 1449. Tin organic compound8 ( DRUCE) 758. If. Unsaturated compounds formation of, from halogenated open-chain com-pounds (INGOLD) 305 961 ; (FAahfER and INGOLD) 2001. V. Valency electrochemical theories of (FRIEND) 1040. arid co-ordination (HRIGGS) 1876. Velocity of reaction in mixed solvents BOROUGH) 970. iuvolving gases influence of colloids on (FINDLAP and THOMAS) 170. Y. Yeast factors influencing the growth of (CASHMORE MCCOMBIE Wld SCAR-(SLATOR) 115. z. Zinc reduction of acid solutions of ferric sulphate by (SUGDEN) 233. Zirconium separation of from colum-binin and from tantalum (SCIIOELLER and POWELL) 1927

ISSN:0368-1645    

DOI:10.1039/CT9211902148

出版商:RSC    

年代:1921

数据来源: RSC

摘要:

FORMULA INDEX. THE following index of organic conipounds of known empirical formula is arranged according to Richter’s system (see Lexikocon der Kohlenstoj- Verbiiulwzgen). The elements are given in the order C H 0 N C1 Br I F S P and the remainder alphabetically. The cotnpounds are arranged-Firstly in groups according to the number of carbon atoms (thus C group, C group> etc.). Secondly accordiug to the number of other elements besides carbon contained in the molecule (thus 5 IV indicates that the rnolecule contains five carbon atoms and foiir other elemou ts). Thirdly nccording to the nature o€ the elements present in the niolecnle (given in the above order). Fourthly according t o the number of atoms of each single element (except carbon) present in the molecule.Salts are placed with the compounds from which they are derived. The chlorides, bromides iodides and cyanides of quaternary ammonium bases however are registered as group-substances. C1 Group. CH Methane ignition of mixtures of air and (MORGAN and WHEELER) 241 ; lability of halogen atoms in suhstituted nitro-derivatives of (MACBETH and PRATT) 1356 ; synthesis of the polyacetic acids from (hWIJ)) 341 ; (INGOLD and POWELL) 1222 1869 ; (INGOLI and PERREN) 1582 1865. CC14 Carbon tetrachloride purification and condensations of (INGOLD and TKORFE) 1227. 1 11 CHCls C h l or0 form additive compound of 4’-dimcthylamino-2-hydroxydistyryl CH,O Formaldehyde photosynthesis of (BALY HEILBRON and BARKER) 1025. CHsOa Formic acid preparation of (COFFEY and WABD) 1303.CHJ Methylene iodide preparation of (PERKIN and SOAKBOROUGH) 1408. CHBS8 T r i t h i o c a r b o n i c acid salts of (YEOMAN) 38. CH& P e r t h i o c a r b o n i c acid salts of (YEOMAN) 38. CHO,NI Nitroform preparation of halogen derivatives of (MACB~TII and PRATT), 354 ; colorations produced by substituted derivatives of (GRAHAM and MACBETH), 1362. Thiocarbsmide additive compounds of azonintn iodides with (SINGH and LAL) 210. ketone with (HEILBRON and BUCK) 1510. 1 111 CH,N,S CH,N,S Dithiocarbazinic acid and its salts (LOSANITCII) 763. CO,NCl Chloropicrin preparation of (ORTON and McKIE) 29. CO,N,Cl C h l o r o t r i n i t r o i n e t h a n e (MACBETH and PHATT) 354. C2 Group. C,H Acetylene explosion of nitrogen and (GARNER and MATSUNO) 1903 ; C,H E t h y l e n e propagation of flame in mixtures of air and (CHAPMAN) 1677 ; action of mercuric chloride with (JENKINS).747. action of sulphur nionochloride with ( MANN POPE and VERNON) 634. 215 2 11-3 111 FORMULA INDEX. 2 I1 C,H,O Acetic acid equilibriuin of aniline with (O’COKXOR) 400; additive compounds of with benzene and 4’-dimethylamino-2-hydroxydistyryl ketone (HEILBROK and BUCK) 1511. C,H,I E t h y 1 iodide volocity of reaction of sodium p-naphthoxide and (COX), 149. C,H,O E t h y l alcoh 01 additive compound of 4’-dimethylamino-2-hydrox~-distyryl ketone with (HEILBROX and BUCK) 1518. CaHllN 2 111 CJOCI Chloral condensation of cresotic and gallic acids with (ALIMCHANDANI C$I,O,CI Dichloroacetic acid preparation of esters of (CBOMPTON and C*H,CI,As B-CIilorovin yldicliloroarsine (GREEN and PRICE) 451.C,H,ONa Sodium ethoxide action of carbon tetrachloride with (INGOLD and C,H,O,N E t h y l n i t r a t e preparation of (HEPWORTH) 254 ; action of diethyl-C,H,BP,Sn E t h y l s t s n n i c t r i b r o m i d e (DRUCE) 761. C2H60S C,H,02Sn E t h y l s t a r i n i c acid and its salts (DRUCE) 758. C&O$ Diethylamine action of ethyl nitrate on (GIBSON and MACBETIX) 441. and MELDRUM) 201. TRIFFITT) 1874, €‘OWELL) 1228. amine on (GIBSON and MACBETH) 441. Monothioethylene g l y c o l (BENNETT) 422 ; condensation reactions of (BENNETT and WHIXCOP) 1860. E t h y l hydrogen s u l p h a t e equilibrium of the formation of (DUNNI-CLIFF and BUTLER) 1384 ; potassium salt dimorphism of (HAMMICK and MULLALY) 1802.C,H,HpSS Me t h y 1 d i t h i o ca r b azin a t e ( LOSANITCH) 764. CrH6NpS~ 8 u 1 p h i d o d i t h io c a r b a mi d e dihydrochloride of (NAIK) 1168. CaHsITl C,H,I,Te Dime t h y l t e l l u r o n i u m di-iodides crystallography and pharma-C,H,I,Te Dim e t h y l t e 1 l u r onium t e t r a i o d i d e (VERNON) 695. CSH,ON &?-Dimethylhydroxylamine and its salts (HEPWORTH) 266. GHlOTl T h a l l i u r n d i m e t h y l h y d r o x i d e salts of (GODDARD) 674. C,H,Cl,Sn E t h y l c h l o r o s t a n n i c acid and its salts (DRUCE) 761. C2H,0,Te Dime t h y 1 t e l l u r o n i u m d i h y d r o x i d e nitrates Of (VERNON) 694. 2 IV C,H,02C1Br C,H,03C1S T h a 11 i um dime t h y 1 i od i cl e ( GODDARD) 674. cological properties of (KNAGGS and VERNON) 105.C h l o r o b ro m oac e t i c a c i d preparation of eeters of (CROMPTON and TRIFFITT) 1874. C h l o roe t h a nesu l p h on i c acid sodium salt (BENNETT) 420. @3 Group. C3H Propylene action of sulphur monochloride on (COFFEP) 94. 3 I1 C,H,Cl A l l y l chloride preparation of (COFBEY and WARD) 1305. CaH60 Acetone action of ammonia on (PATTERSON and MCMILLAN) 269, C3H602 A l l y l alcohol preparation of (COFPEY and WARD) 1303. E t h y l formate influence of neutral salts on the hydrolysis of (NANNIXG), 2079. M e t h y l acetate rate of hydrolgsis of (Bu~~Rows) 1798. 3 111 C3H,03Na co-Sodium glyceroxide (FAIRBOURNE and TOMS) 1036. C3H,IA$ 2156 Methylethyliodoarsine (BURROW and TURNER) 433 FORMULA INDEX. 3 IV-5 I11 3 IV C3H6O2N2Br Bromomalonamide (BACKES WEST and WHITELEY) 364.c,&O8c1S Chloropropaneaulphonic acid barium salt (COFFEY) 96; (Pol% and SMITH) 398. Cp Group. C,H,Os Ally1 formate preparation of (COFFEY and WARD) 1303. C,H,O T a r t a r i c acid decomposition of by heat (CHATTAWAY and RAY) 34 ; complex cupric salts of (PACKER and WARK) 1348. C,H,Os E t h y l acetate additive compoun’d of 4’-dimetliyla1nino-2-hydroxy-dlstyryl ketone with (HEILBRON aud BUCK) 1510. C H 0 E t h y l ether solubility of in solutions of sodium chloride (TEORNE), l:L.o 4 I11 C4H,C1,As BB’-D i c h 1 or odi vi n y 1 c h 1 o ro a r s i n e (GREEN and PRICE) 452. C,H,0Ci2 rB-Dichlorovinyl e t h y l e t h e r preparation of dichloro- and chloro-C,H,ON cycZoPr op a n o n e s e m i c a r b az o n e ( INGOLD) 329.C,H8ClZS BB’-D i c h 1 or0 d i e t h y 1 d i s u 1 p 11 i d e (BENNETT) 418. C4H,Cl,Ss BB’-D i c h lo r o d i e t h y 1 t r i s u 1 p h i d e (MANN POPE and VEBNON), 639. C4Hl10Tl T h a l l i u m d i e t h y l hydroxide salts of (G~DDARD) 675. 4 IV C4Hs0,NaS N-S u 1 p h i do b i s ace t a mid e (NAIK) 1167. C,HRO,N,Br Bromomslo ndimethylamide (BACKES WEST and WHITELEP), 565. bromo-acetates from ( CROYPTON and ‘I‘RIFFITT) 1874. C,H,O,ClS B-Chlorobutane-y-sulphonic acid barium salt (POYE and SYITB), 399. C,H,,OI2Te2 Di-io do t e t ram e t h y 1 d i t e l l u r on i II m o xi d e ( VERXON) 691. C4H1,ON4C1,Co 4 v trans-D i c h l o r o li i e t h y 1 en e d i a m i n e co ba 1 t i c hydroxide, salt8 of (DUFF) 1987. Ca Group. C6Ha04 C,H,N Pyridine additive compound of 4’-dirnethylamino-2-methoxgdistyryl C,H,O cycZoPropanol-l:2-dicarboxylic acid and its silver salt (INGOLD) 328, C,H,O Lactonic acids of aa‘-dihydroxyglutaric acids and their silver C,H,O a-Hydroxyglutaric acid (INGOLD) 318.C,H,OI ad-Di h y drox y g l u t a r i c acids ( INGOLD) 322. CaHnN P i eridine action of on alkyl nitrates (GIBSON and MACBZTE) 438 ; A2-cycZoPropene-l:4-dicarboxylic acid (FARMER and INQOLD) 2015. ketone phenylhydrazone with ( HEILBRON and BUCK) 1520. salts (INGOLD) 322. action o[ on silicon organic compounds ( KIPPING and SANDS) 848. 5 111 C5H,0,Br l-Brom ocyclo p r o p s n e-l:2-di c ar b o x y l i c acid and its ralta (IN-C,H,O,Na 4-N i t r o-3:5-dim e t h y lisoo x azo 1 e (MORGAN and 3oaa~sa) 699.CS€i,04B~s Di brom oglu t a r i c a c i d s (INGOLD) 317. C,H,O,N E t h 1 cyanoacetate syntheses by means of (INGOLD) 329 341; (INGOLD a d PBRREN) 1682 1865 ; sodium derivative condensation of carbon tetrachloride with ( INGOLD and POWELL) 1229. 215’7 OOLD) 325 5 111-6 111 FORMULA INDEX. C,H,02N hydroxide salts of C,H,0N2 4-Am i n o-3:5-dim e t h y l is0 ox azole and its hydrochloride (MORGAN C,H,,02N C,H,ON,Fe N i t r o p r u s s i c acid and its salts (BUI~ROWS and TURNER) 1450. C,H,ONI C,H,02Br2Te T e 11 u r i u m ace t y l a c e t o ne d i b r o in i d e (MORGAN and DREW), 616. C,H,O,I,Te Tellurinm a c e t y l a c e t o n e di-iodide (MORGAN and DREW) 617. C,H,02N2S2 Di t h iomeso xoJ ini e t h y l a mide (NAIK) 384. 3:5-Di m e t h y 1 is00 xa z 01 e-4-d i az o n i u m (MORGAN and BURGESS) 702.and BURGESS) 700. C holine crystalline preparation of (DUDLEY) 1260. 5 IV 4-1 od o-3:5-dim e t h yliso o x az ole (MORGAN and BURGESS) 1547. C Group. C,He Benzene adsorption of by charcoal (BAKK and KIXG) 464 ; chlorination of with sulphuryl chloride ( SILBERRAD) 2029 ; additive compound of 4’-dimethylaniino-2-hydroxydistyryl ketone with (HEILBRON and BUCK) 1510. C,H12 S-Eth yl-Aa-butylene (KoN) 821. 6 I1 C6H,02 p-Benzoquiiione additivi compound of 4’-diinethylamino-2-hydr-C,H,O Phe n o 1 additive compound of 4‘-dirnethylamino-2-11ydroxydistyryl ketone C,H,N Aniline equilibrium of acetic acid with (O’CONNOR) 400 ; velocity of C,H,O M e t h ox ycyclo p 1-0 p a n e-l:2-d i c a r b ox y li c acid aud its silver salt CaHlnOs B-Glucos an preparation and relationships of (IEVINE and OLDHAM), oxydistyryl ketone with (HEILRRON and BUCK) 1511.with (HEIcI~I~ON and BUCK) 1511. reaction of w-bronioacetophenone and (Cox) 145. (IKGOLD) 327. 1744. a-Methoxyglutari c acid and its silver salt (INGOLD) 320. C6H,,N3 $-&Met h y 1 am i n o e t h y 1 g 1 y o x a l i 11 e and its salts ( FARGHEK and C6H1206 Dextrose mutarotation of and its catalysis by metals (GARNER arid C,Hl,N Hexaniethylenetetramine compounds of with metallic salts and PYMAN) 734. JACKMAN) 1936. acids (lt.4~ and SARKAR) 390. 6 I11 C,H30,N s-‘I? r i n i t rob e n z e ne additive cornpounds of with 4’-dimethylamino-2-ilydroxydistyryl ketone and 4’-dimetbylamino-2-metlioxydistyryl ketone ( HEIL-BRON and BUCK) 1511.CsH30,N Picric’ acid preparation of (KING) 2105 ; equilibrium of 5-phenyl-acridine with ( BA~SETT and SIMMONS) 416. CoH,012Fe C6H4O4N8 m-Dini trobenzene additive compounds of with P‘-dimethylamino-2-hydroxydistyryl ketone and 4’-dimethylamino-2-methoxydistyryl ketone (HEILBRON and RUCK) 1511. CsH40,N2 D i n i t r o p h e n o 1 s influence of position on the solubility arid volatility of (SIDGWICK and ALDOUS) 1001. C6H,0,N N i t r o p 11 en o 1 s influence of position on the solubility and volatility of (SIDGWICK and ALDOUS) 1001. CaH,Br2Bi P h enyldibromobisinu t h i n e preparation of (CHALLENGER and ALLPRESS) 919. C,Hs02Ns N i t r o a n i l i n e s solubility and volatility of (SIDGWICK and RUBIE), 1013. F e r r i o x a l i c acid potassium salt (THOMAS) 1140.215 FORMULA INDEX. 6 111-7 I1 CeHaNCl Chloroanilines solubility and volatility of (SIDGWICK and RUBIE), 1013. CJ&C1.& CaH,ON BB'B"-Trichloro t r i v i n y l a r s i n e (GREEK and PRICE) 452. 8-P h en y 1 h y d r ox J l a min e preparation of from nitrohenzene (LAPWORTH and I-Benzildioxime (ATACK and WHIKYATES) 1184. PEARSON) 765. CaH804Brg CeH,0J2 CdHsNI M e t h y l p y r i d i n i u m iodide mercuri-iodide of and its crystallography CeHI2NaS Met h y 1 b i s m e t h y 1 d i t h io c a r b a m a t e (LOSANITCH) 765. CsH,2C12S Bfl'-Dichlorodi-~~~-propy1 s u l p h i d e (COFFEY) 97 ; (POPE and SMITH) 397. CsH,,ClaS3 E t h y l e n e bis-6-chloroe thy1 s u l p h i d e (BENNETT and WHINCOP), 1862. C6H,,0aS @'-D i h y d r o x y di-n-p 1-0 p y 1 s u l p h i de ( COFFEY) 96.CeH,,02Sz E t h y l en e bis-8-h y d P o x y e t 11 y 1 s u 1 p h i d e (BENNETT and WHIN-Dibromoadipic a c i d s (PERKIN and ROBINSON) 1392. D i - i od oad i pic acids (INCOLD) 964. (PORTER) 1770. COP) 1862. 6 I V C,H,ONCl o- and m-C h 1 o ro n i t r o 9 o b e n z e n e s (HAWORTH and LAPWORTH), C,H,O,NS 6-Nitrophenol-o-sulphonic acid and its salts (KIKG) 1417. C,H,ONCl m-C h 1 or0 ph e n y 1 h y d rox y 1 am i n e (HAWORTH and LAPwoRrH), 773. CJ3,OJ?,C1 2-Chl o ro-5-ni t r o p h en y 1 h y d r a z i n e (PERKIN and PLANT) 1837. CeHaOeN$ C,H,O,NS C6H80,N,S C,H,s021,Te Di-iodo h e xame t h y l t r i t e l l u r o n ium d i o x i d e (VERNON) 690. C,H80sNSAs 3-A m i n o-4-h y d r o xy-5-s u 1 p h i n op h en y 1 a r s i n i c a c i d (KING), 1113.C,H,O,NSAs 1114. 772. N i t r o am i no p h e n ol-o-su 1 p ho n i c acid s (KING) 1418. 6-A m i n o p h e n o 1-o-s u 1 p h o n i c a c i d (KING), 1117 1417. 4:6-D i am i n o p henol-o-s ul p hon i c a c i d (KING) 1419. 6 V 3-Am i no-4-hydro xy-5-aul p h o p h en y l a r s en io u s acid (KING) 1420. 3-A m i n o-4-h y d r oxy-5-9 u 1 p h o p h e n y 1 a r s i n i c aci d (KING), C Group. C7Hs To1 uen e sulphonation of with chlorosulphonic acid (HARDING) 1261. C,H,O Ben x a 1 d e h y d e condensation of m-dimethylaminophenol with ( KRISHNA POPE) 286. C,H,o2 Salicylaldehyde additive compounds of 4'-dimethylamino-2-hydroxy-C,H,06 G a l l i c acid condensation of chloral with (ALIMCHANDANI and MEL-C,H,C1 m-Chlorobenzyl c h l o r i d e (KENNER and WITHAM) 1460.C,HB02 Dime t h y l p y r o n e action of iodine and barium hydroxide on (COLLIE C,H,O Anhydro-acid from methane t r i a c e t i c a c i d (INGOLD) 353. C,H,N 1 :l-D i m e t h y 1 @opr o p R ne-2:3-di c a r b o x y 1 on i t r i 1 e (BIRCH GOUGH, C;H,,O ci8- and tra?zs-l:l-DimethylcycZopropane-2:3-dicarl~oxylic a c i d s 7 I1 distyryl ketone with (HEILBRON and BUCK) 1512. DRUM) 201. and REILLY) 1550. and KoN) 1322. (BIRCH GOUGH and KoN) 1322. 21 5 7 11-7 IV FORMULA INDEX. C,H,,O M e t h a n e t r i a c e t i c acid preparation of (INGOLD) 352. C,H,,O D i e t h y 1 m alo n a t e sodium derivative condensations of aS-unsatu-rated esters with (IKGOLD and POWELL) 1976. 7 I11 C,H,O,N Nitro-3-keto-l:3-d ihydroindnzoles and their sodium salts (KEN-C,H,O,N 2:4-Dinitro-m-tolylazoimide (BRADY and BOWMAN) 898.C,H,O,N 2:4:6-Trinitrotoluen e additive compound of 4’-dimethylamino-2-C,H50,N T r i n i t r o ph en y 1 m e t h y 1 n i t r o a m i n e (tetryZ) thermal decomposi-C,&O,N T r i n i t r oh y d ro x y p h e n y 1 rn e t h y 1 n i t r oa m i n e thermal decompo-C7H,03N4 4-N i t r o-l-h y d r o x y m e t h y 1-1:2:3-b e n z o t r i a z ole 8 and C,H,O,N 2:4-Din it rotoluene additive compound of 4’-dimethylamino-2-bydr-NER and WITHAM) 1055. hydroxydistyryl ketone with (HEILBRON and BUCK) 1511. tion of (HINSHELWOOD) 722. sition of (HINSHELWOOD) 722. (BRADY BOWMAN) 898. oxydistyryl ketone with (HEILBRON and BUCK) 1511. Dinitrotoluenes partial reduction of (BURTON and KEKNER) 1047.C,H,ON 5-Am i n o-3-k e t o-1:3-d i h y d r o i n dazo le and its hydrochloride (KEN-C7H,0,N3 N i t r o f o r m a1 d e h y d e ph en y 1 h y dr a zo n e tautomerism of (SIDG-C,H,O,I Subs t a n c e and its salts from dimethylpyrone barium hydroxide, C,H,NS P h e n y 1 d i thi o c a r baniic acid hydrazine salt (LOSANITCH) 765. C,R,Cl,Bi p-To1 y l d i c h 1 or o b i s mu t h i n e (CHALLENGER and ALLPRESS) 917. C,H,02N2 2-Nitro-m-toluidine (BURTON and KENNER) 1052. C,H,O,N D i n i t r o t o l y l h y d r a z i n e a (BRADY and BOWMAN) 894. G,H,0,Br2 cis-l:3-D i br o m ocycZope n t a n e-1:3-d i c a r b o x y 1 i c a c i tl C,H,N,S FIi e n y 1 d i t h i o c a r b a z i n i c acid hydrazine salt (LOBANITOH) 765. C,H,O,N Caronimide (BIRCH GOUCIH and KoN) 1322.C,H,N,Cl 2-C h l oro-3:4-t 01 y l e n e d i a ni i n e (MORGAN and GLOVER) 1706. C,H,,ON m-Met hoxyphenylhydrazine (KERMACK PERKIN and ROBLN-C,H,,O,N 4-A c e t g l am i n o-35-d im e t h ylisoox a z ole (MORGAN and BURGESS), 701. C7H1004Brs &I e t h y 1 ad-di b r o mogl u t a r a t e ( INGOLD) 317. C,H,,NI E t h y l p y r idiniurn iodide mercuri-iodide of and its crystallography Methyl-a-picolinium iodide mercuri-iodide of and its crystallography C7H110eNI dl-a-M e t h y 1 am i n o-B-gl y 0x8 line-4-pr o pi0 nic aci d and its salts C7H,,0sN E t h y 1 u-c a r b a m y l c r o t ona t e (GUPTA) 303. C,H,,O,N Glycylch oline and its salts (DUDLEY) 1256. C,H,O,N,Cl 3-Chloro-5-nitroindazole (KENNER and WITHAM) 1057. C,H,O,NCl 0-C h lor0 d i n i t r o t o 1 u en e s (MORGAN and JONES) 187.C,H50sClIS 2:6-D i c hlor o-p- t o l u e n esu 1 p h o n y1 c h l o r i d e (DAVIES) 872. C,&O,N,Cl 3-Chloro-2:4-dinitrotoluene (BRADY and BOWMAN) 897. NER and WITHAM) 1056. WICIK and EWBANK) 491. and iodine (COLLIE and REILLY) 1553. (PERKIN and SCARBOROUGH) 1407, SON) 1640. (PORTER) 1770. (PORTER) 1772. (FARGHER and PYMAN) 736. 7 IV 8-Chlorodinitrotoluenes (MORGAN and CHALLENOR) 1537 ; (MORUAN and GLOVER) 1700. 216 FORMULA INDEX. 7 IV-8 I1 C,H,O,N,I C,H,ON,Cl and its C7HaOaNC1 p-Nitrobenzyl chloride condelisation of nitroso-compounds with C7HeO&1,S 2-C h loro-p-t o 1 ue n es ul p hon y 1 chloride preparation and nitra-3-1 od o-2:4-d i n i t r o t olu en e (BRADY and BOWMAN) 897.4-C h l or o-l-h y d r o xy-5-in e t h y 1-1 :2:3-b e n z o t r ia z o 1 e, hydrazine salt (MORGAN and GLOVER) 1705. (BARROW and GRIFFITHS) 212. tion of (DAVIES) 860. 6-Chloro-o-toluenesulphonyl chloride (DAVIES) 878. C,H,O,NCl 2-Chloro-5-nitro-p-cresol and its salts (DAVIES) 866. C,H,O,Cl,S 2 6 D i c hlor 09-t 01 u enesul p h o n i c acid and its salts (DAYIES), 872. C,H,O,N,Cl 2-Ch lo r 0-3:5-dini t r o-p-t 01 ui d i n e (DAVIES) 868. C,H,NClBr 6-C hloro-2:4-di br om o-m-tolui d i n e (DAVIES) 866. C,H702N2C1 2- and 6-Chloro-4-nitro-m-toluidines (MORGAN CHALLENOR and C,H,O,ClS o- andpToluenesulphony1 chlorides melting points of mixtures C,H,O,,ClS 6-Chloro-o-toluenesulphonic acid and its salts (DAVIES) 879. C,H,,O,Cl,Te Tellurium O-ethylacetylacetone trichloride (MORQAN and DREW) 613.C,HI2O2N2Br Di bromomalondiethylamide (BACKES WEST and WHITE-LEY) 367. C7HI80,N,Br B ro m om a1 on d i e t h y lam i d e (BAUKES WEBT and WHITELEY), 366. C,H,O,NClS 6-C h l o r o-o-b e nzoi c BU 1 p h i n id e (DAVIES) 880. C,H,O,NClsS Ch lor on i t ro-o- and - p t o l u e n e s u l p hon y 1 chlorides (DAvIE~), C7H,O,NC1S C hlor oni t r o-o- and -pt o l uene s u l p hon ic acids and their salts C,H,O,NCl,S 2:6-D i c h 1 or o p t o 111 en e s u l p h o n a m i d e ( DAPIES) 872. C7HS0,N,ClS C h l o ron i t ro-u- and -pt oluen esulp h o n am i de s (DAv~Es) 865, 870 884. C,H,O,NClS 6-C h 1 or o-o-t 01 ue n e s u 1 ph o namide (DAVIES) 879. C,H,O,NClS 6-C hlo ro-m-t o l u id ine-4-su 1 p h on i c aci d (DAVIES) 865.JONES) 1544 ; (MORGAN and GLOVER) 1704. of (HARDING) 260. 7 v 864 870 884. (DAVIEa) 866 870 884. C Group. CeHle 1:l-Dimethylcydohexane from methylheptenone(CRosaLEP and RENOUF), 271. 8 I1 C,H,O Car b ox y m ethane t r i ac e t i c d i anhydride ( INGOLD and POWELL), C,H,02 An isaldehyde additive compound of 4’-dimethylamino-2-hydroxy-1873. distyryl ketone with (HEILBRON and BUCK) 1612. Phenyl acetate action of sodium on (PERKIN) 1284. C,H,O Cresotic acids condensation of chloral with (ALIMCHANDANI and C,H,N 6-Am i n o-5-m e t h y l i n daz o 1 e (PEARMAN) 718. CsH,,Os Lac t on e of 8-h y d r o x y-B-m e t h y 1 b u t a n e-y86-t r i c a r box yl ic acid cis- and trans-cycloPen t ane-1:2:3-t ric ar box y l i c a ci ds synthesis and resolu-MELDRUM) 201.(BIRCB GOUGH and KoN) 1323. tion of (PERKIN and ROBINSON) 1392. C8Hl0O8 n-B u t ano-uSy8-t e t r acar bo x y l i c acid (INGOLD) 348. 216 8 11-43 111 FORMULA INDEX. C,H,,O Carboxymetlianetriacetic acid and its salts (IXGOLD and POWELL), C,H,,As P h e n y l d i m e t h y l a r s i n e additive compounds of with arsenic and C,H,,O eycZoPen tenylacetoiie (Kox) 823. C,H,,O E t h y l cyclopen t a n o n e-3-ca1.b o xy l a t e (INGOLD and THORPE) 500. c&O4 cycZoPe n t ane-l-ace t i c-1 -c s !.b o s y I i c acid ( N O ~ R I S and TIIORPE), C,H,zOs w - M e t h y l m e t h a n e t r i a c e t i c acid (INGOLD and PERREN) 1599,1868. c,H,4o Ketone froni B6-diethylglutaric acid (ICON) 821, C8H,,0 1C e t o n e from reduction of k e t o n e C,H,,O (KoN) 822.C,H,,S T e t r a m e t h y l d i e t h y l e n e d i s u l p h i d e (POPE and Snzrm) 400. 8 I11 C,H,O,N, C8H,0aCl 4-Chlorophthali c acid preparation of (MOORE MARBACK aud C,HsNC1 3-Chloro-2-cyanobenzyl c h l o r i d e (KENNER and WITHAM) 1458. CsH,OS 3 - 0 x y ( l ) t h i o n a p h t h e n preparation arid derivatives of (SMILES and CsHaO,N €I ydan t oin from 6-c a r b anii d o-m-h y d r o x y benzoic a c i d ( FROE-C,H,NCl 3-C h 1 o r o-a-t o 1 u o n i t r i l e ( KENNER and WITHAM) 1458. C,H,OBr w-€3 r o m o a ce t o p h c no n e velocity of reaction of aniline arid (Cox), 145. CsH,O,C1 3-Chloro-o-toluic a c i d (KENNER and WITHAM) 1458. C,H,O,N 2:4:6-Tri n i t ro t 01 ylni e t h y l n i t r 0 s oamine ( RRADY and GIBSON), C,H,0,N5 2:4:6-Tri n i t r o t 01 y 1 me t h y I n i t r oa m i n e (BRBDY and GIBSON) 98.C8H,N,C1 5-Chloro-&methylbe nziminazole (MORGAN aud CHALLENOH), 1542. C,H,O,N a c i tl (BIRCH GOUGH arid KoN) 1320. C,H,02S m-Methylthiolbenzoic '"acid (SMILES and STEWAR'I') 1797. C,H,03N2 664. 1869. phosphorus iodides and metallic iodides (BURROWS and TURNER) 1449. 1208. cycZoP e n t y 1 a c e t o n e ( KoN) 824. 6-N it ro-3:4-m e t 11 ylene d iox y benzoni t r i l e (KSFFLRR) 1478. PROUD) 1788. MCCLELLAND) 1810. LICHER and COHEN) 1432. 104. 2:3-D i cyano-1:l-d i rn e t h y 1 cyclo p r o pa ne-2-c a r box y 1 i c o-Carbamidobenzoic acid preparation of (SUO'I'T and COHEX), N i t r o a c e t a n i l i d e s soluhility and volatility of (SIDGWICK and RURIE) 1013. Car barn i Li o-m-h y d r o x y b en z o i c a c i d s (FROELICHER and COHEPJ), ( BRADY and C8&OoN, 14 30.CsH,04N, BOWMAN) 899. C,H,O,S C,H,O,N D i n i t r o t o l y l m o t h y l n i t r o s o a m i n e s (RRADY and GIBSOX) 103. C,H,0sN2 CsH,OeN D i n i t r o t 01 y l m e t,h y1 n i t r oa 111 i n es (BRADY and GIBSON) 103. CaH,N3C1 6-C h l o r o-2-m e t h yl-2:3-t o 1 y 1 e n e d i a z oi m i n e (MORGAN and JONES), 191. CsH,ON 2:3-Dicyano-l:l-di in e t h ylcyclopropa ne-2-car box y 1 amide (BIRCH, GOUGH and KoN) 1320. C,H901N Amino-m-methoxybenzoic a c i d s (FROELICHER and COHEN) 1430. C,H903N3 Ace t y 1-p-ni t ro p h e n y 1 h y d r a z i n e (MORGAN and DREW) 622. CsH,O,N D i n i t r o m e t h y l t o l u i d i n e s (BRADY and GIBSON) 101. 2162 P o r m a l deh yde-2:4-d i 11 i tro-m-t o l g l h y drsxo n e m-Methylsul phonebenzoic acid (SIMILES and STEW-ART) 1797.2:4-Dini t r o p hen y 1-6-11 y d r o xye t h y 1 e t h e r (PAIREOURNE and TOMS) 2077 FORMULA LNDEX. 8 111-8 V C,Hl,ON 6-A niin o-2:3-di h y d r 0-1 :4-ben z isooxaz i n e ( FAIRBOURNE and C,H1,02N2 p-Am i n o p h e n y l a m i n oa c e t i c acid hydrochlorides of (GRAKT and CeHllON m-Dimethyl aniinophenol condensation of benzaldehyde with CBHl,O,N cyclo P e n t a n on e-3:4-dic a r b o xy 1 i c acid semi c a r b a zon e (IKCOLD), C,H,,N,CI 6-c h 1 oro-2-me t hyl-2:3-tolyl en e d iam ine (MORGAN a i d JONES), (MORGAN and CHALLEKOR), Ethyl-a-picolinium iodide mercuri-iodide of and its cryjtallography Prop y 1 p y r i d i n i n m i odi d e mercuri-iodide of a11d its crystallography TOMS) 2078.PYMAX) 1901. (KBISIINA and POPE) 286. 350. 191. 1542. (PORTER) 1772. (PORTER) 1771. 6-C h l o r o-3-N-m e t h yl-3:4-t 01 y 1 an e d i a rniue C,Hl,NI C,HlsO,N C,H,,ON C,Hl6C1,S C,H,,ON l - E t h o x y m e t h y l p i p e r i d i n e preparation of (McLEon and 8 IV E t h y 1 cyan o m e t h y l b u t y r a t e s ( INGOLD) 339. BB’-Dichlorodi-sec.-bii t y l s u l p h i d e (POPE and SMITH) 399. Oxitne of k e t o n e C,H,,O (KoN) 822. ROBINSON) 1474. C,H,0,N2C1 Subs t a n c e from sodium hypochlorite and 2:4-diketo-1:2:3:4-tetr.a-C8HsO4NC1 Id e t h y l 2-12 h l o r o-3-ni t r o b e n z oa t e (KENYER aiid SIXTBBINGS), C,H,ONCl Chloroacetanilides solubility aiid volatility of (SIDGWICIZ and hydroquinazoline (Scow and COHEN) 665.598. RUBIE) 1013. 3-Cliloro-o-toluainide (KENNER and WITHAM) 1458. C,H,O,N,Cl (MORGAN and C,He0,N2S 2:4-Dini t r o ph an yl 8-h y d r ox y e t h yl s u 1 p h i d e (BENNETT and CBH,OeNaC1 C h l or 0 n i t r 0 -3-rne t h y 1 t 0 l u i d i n e s (MORGAN and JONES) 189. C,H,,02C1Br 4-C h 1 o r o-4-b porn o-1:l-d i m e t h ylcycloh e x a n e-3:fi-di 0 n e C,Hl,O,NT1 T h a l l i u m d i met h y 1 n i t r o p h en o x i d es (GODDARD) 1812. C,Hl,,O,N,T1 T h a l l i umdime t h y l C,Hls02N,S N-S ul p h idob i s b u t y r a m i d e ( NAIK) 1168. C,H&,C1,S BB'-Dichloro-di-set.-butylsul ph one (POPE and SMITH) 399. CEHleO& C h 1 or o n i t r o t o 1 y 1 u1 e t h y 1 n i t r o s oa m i nes JONES) 189. WHINCOP) 1864. ( N o a ~ I s and THORPE) 1210.4:6-di n it r o-2-an] in o p h e n o x id e (GOD-DARD) 1313. S u l ph i d obi s-8-h y d r o x y d i e t h y l s u l p h ide (BENNETT and WHINCOP) 1863. C,H,,O,N,Co cis- bl a 1 e a t o d i e t h y l e n e d iam i n e c ob n 1 t i c h y d r oxide salts of (DUFF) 388. C8He105N4Co cis-S u c c i na t o d ie t h y l e n e d i a m ine c o ba 1 t i c hydroxide salts C,H2,0,N4Co cis-M e s o t a r t r a t o d i e t h y l e n e d i a rn i n e co b a 1 t i c hydro x ide, 8 V of (DUFF) 357. salts of (DUFF) 388. C,H,O4NtC1S 2:4-D i n i t rop hen y 1 8-c h 1 o roe t h y 1 su lp h i d e (BEKNRTT and C,H,O,N,BPS 2:4-Di n i t r o p he n y 1 @-br o m o e t h y 1 s u l p h i de (BENNETT and WHINCOP) 1864. WHINCOP) 1864. 216 8V-9 I11 FORMULA INDEX.C,H,O,N,ClS 2:i-D i n i t r o p h e n y 1 8-c h 1 or0 B t h y 1 s u l p h o xid c (BENNETT C,H,O,N,BrS 2:4-D i n i t r o p h any 1 B-b rom oe t h y 1 s u l p h o x i d e (BENNETT CsH1,O,NaBrCo b ro mid e C,Hl,04NdBP3C0 cis-D i b r o m o 8 uc c i na t od i e t h y l e n e d i am in e c o b a 1 t i c C,H,,O,N,Br,Co eis-Di b r o mo s u c c i n a t o d i s t h y l e n e d iam i n e c o b a1 t i c C,H,,O,N,BrCo cis-S 11 c c i n a t o d i e t h y Zen e diain i n e c o b a1 t i c bromide C,H,,O,N,BrCO cis-M e s o t a r t r a t o d i e t h y 1 e n e d i amin e c o ba I t i c br o mid e and WHINCOP) 1864. and WHINCOP) 1864. cis-M a1 e a t o d i e t h y l e ne diam i n e c o b a1 t i c ( + 2H,O) (DUFF) 388. bromide (-f- 2H20) (DUFF) 359. hydroxide (DUFF) 389.(f 2H,O) (DUFF) 387. (+ 2H,O) (DUFF) 388. C,H,N 4-Phenylglyoxaline and its salts (GRANT and PYMAN) 1896. C,Hlo03 A t r o l a c t i n i c acid resolution of (WREN and WRIGHT) 798. C9Hlo04 P h e n y l g l y c e r i c acid action of fused potassium hydroxide on CQHloN 5-Amino-pam mi n o p he n y l g 1 y oxal i ne dihydrochloride of ( GRAXT CoH,,Os eycZoH e xane-l-ac B t ic-l-ca r box y l i c an h y d r ide (NoRRrs and C,HlaO Acid from oxidation of cyelohexane-1 :l-diacetic acid ( h a o m and C9Hld04 cyc7oH e x a n e-l-ac e t ic-l-carb o x y 1 i c acid and its silver salt ( NORRIS C9Hl10 T r i m e t h y l s a c c h a r o l a c t o n i c a c i d (IRVINE and OLDHAM) 1’157. CQHleOs E t h y l a - h y d r o x y g l u t a r a t e (INGOLD) 318. a- H y d ro x y-8-ph e n y 1 pro pi0 n ic acid {WREN and WRIGHT) 798.(h SUEUlt and WOOD) 1697. and PYMAN) 1900. THORPE) 1206. POWELL) 1870. and THOXPE) 1206. Trinie t h y 1 B-glucosan preparation of (IRVINE and OLDHAM) 1754. 9 111 3:4:5-Tr i h y d r o x y-2-t r i c h 1 o r om e thy 1 p h t h a l i d e C,H,O,Cl (ALIMCHAN-C,H,0,N2 Dike t o t e t r a h y d ro q ui naz ol i n e c a r b o xy 1 i c a c i d and its sodium C,,H804N4 5-Nitro-4-p-nitrophen ylglyoxaline and its nitrate (GBANT CoH,OC1 CvH,0,Ns 4-Nitrophenylglyoxalines and their salta (GRANT and PYMAN), 1897. C,H,O,N 5-Ni t PO-4-p-h y d r o x y ph en y lg 1 y oxa l i n e (GRANT and PPUAN), 1902. CQH,OIN Ace t y 1 derivative of 5-n i tro-3-k e t 0-1 :3-di h y d r oindaz 01 e (KENNER and WITHAM) 1055. CQH,0,N4 5-Ni t r o-4-p-am i no p h e n y lg 1 y oxaline and its dihydrochloride (GRAKT and PYMAN) 1901.C,H,04Nt 6-N i t ro vera t r o n i t r i l e (KEFFLER) 1479. C,H,O,N 3-Carbamidophthalic acid (f &H,O) (SCOTT and COHEN) 666. C,HsN,S 2-Thiol-4-phenylglyoxalin e and its salts (GRANT and PYMAN), 1895. CoHoON 6-Me t h o x y i n d o l e (KERMACK PERKIN and ROBINSON) 1632. DANI and MET~DRUM) 208. salt (SCOTT and COHEN) 667. PYMAN) 1898. C h 1 o r o-l-h y d r i n don es ( KENNER and WITHAM) 1459. 216 FORMULA INDEX. 9 I11 C,H,O,C1 1891. 5-C111oro-2:4-d iniethylbenzoic acid (MORGAN and HICKINBOTrOhl), B-nz-C h 1 or o p h en y 1 pro 1) ionic acid ( KENNER and WITHAM) 1460. C,HsO,Br 5-B romo-2-m e t hox yp h a n y lace t a 1 d e h y d e (READ and AXDEEWS), C,Hs03C1 Cinnamic a c i d c h l o r o h p d r i n preparation of (READ and C,H,O,Br Cinnamic a c i d bromohydrin and its salts (READ and AXDREW'S), C,HoO,I A c e t y l derivative of s u b s t a n c e C,H,O,I (COLLIE and REILLY) 1554.C,H*O,N o-Nitro-p-methoxyphenylacetic a c i d (KERMACK PERKIN and 1785. ANDREW'S) 1777. 1778. ROBINSON) 1631. 3-Ni tro-2-m e t h oxy-ptol u i c a c i a (SIMOPU'SEN and RAU) 1342. CBHs06N3 45-D i n i t r oa c e t o-o-t 01 u i d i d e (MORGAN and GLOVER) 1703. C,HsOl1C0 Cobaltimalonic acid potassium salt (THOMAS) 1140. CoHoN2Cl 5-C h l oro-l:g-di m e t h y 1 be n z i m i n az o 1 e (MORGAN and CHALLENOIL), 1541. CoHloOINa Malonphenylamide (f 4H,O) (BACKES WEST and WHITELEY), 372. CBHloOsN* 2-Nitroaceto-m-toluidide (BURTON and KENNER) 1052.CSHl0O1N3 Car b am ido-m-m e t h o x y b e nz o i c a c i ds (FROELICHER and COHEN), 1430. 3-Nitro-2-me t h o x y-p-t oluamide (SIMONSEN and Rau) 1342. CBHla04N4 Ace t a l d e hyde-2:4-di n i t r o-m-t o 1 y 1 h y d r a zon e (BP.ADY and BOWMAN) 899. C,HI,O,NS a@-D i c yano-y-h y d r o x y-ym e t h y 1 b u t an e-up-d i car b ox y 1 i c acid, atid Its silver salt (BIRCH GOUCH and KoN) 1323. CsHlo06N Ace t y 1-2:li-din i tro-m-t 01 y l h y d r az i n e ( BRADY and BOWMAN) 897. CaHllON p-Dimethylaminobenzaldehyde additive compound of with 4'-dimethylamino-2-hydroxydistyryl ketone ( HEILBRON and BUCK) 150:. CpH1102N~ p - Ace t y l a m i n on i tros o m e t h y Ian i li n e ( PERKIN and PLAST) , 1835. C,H1103N 3-Amino-2-methoxy-p-toluic acid and its salts (SINONSEN and hU) 1343.B-Hydroxv-8-3:4-methylenedioxyphenylethylamine and its salts (MASON),"I 077. C,H,,04N D i n i t r o d i m e t h y 1 to1 u i din e s ( BRADY and GIBSOS) 102. CoH1204Brs Met h p l cis-l:3-d i bro m o cyclopen tane-l:3-di car box y l a t e (PER-KIN and SCARBOROUGH) 1407. CeHlsONs p-A c. e t ylam i n o p h e n y 1 me t h y 1 h y d r a z i n e ( PERKIN and PLANT), 1836. CgH130,B~ C,Hi,O,Br, CoH14NI Propyl-a-picolinium iodide mercuri-iodide of and its crystalfo-CaH150N3 Semicarbazone of cyclopentenylace tone (KoN) 823. CsHl,OAs P h en y 1 t r i m e t h y l a r so nium CJI,,O,Br E t h y l a-bromoglutarate (ENGOLD) 316. C9H15N21 Phenylmethylethylazonium iodide additive compound of CaHl;ON Semicarbazone of k e t o n e C,H140 (KoN) 821.4 - 8 i t ro-2-car be t hox yp he n y 111 y d r a zi n e ( KENNER and WrTHabr) 1055. E t h y 1 a-bromoglutaconate (FARMER and INGOLD) 2013. E t h y 1 ua'd i b rorn oglu t ar a t e (IKGOLD) 318. graphy (PORTER) 1773. h y d r o x i d e cadmi-iodide of ( RIJRROWS and TURNER) 1449. tlliocarbamida and (SINGH and LAt) 211. Semicarbaxone of cyckpeatylacetone (KoN) 824. 216 9 111-10 I1 FORMULA INDEX. CoHls0,N2 Malon d i - w p r o p y l a m i d e (BACKES W w r and WEIITELEY) 367. CBH190N3 SeIiiicarbazone of ketorio C8H160 (Iios) 829. CDH,o2NC1 5-C 11 l o ro ison i t r 0s o-l-h y d r i n d o n e ( KENNEE and WITHAM) 1461. C,H,O,N,Br D ib r o m o i n a1 o n cl i b r o m o p h e n y l a m i d e ( RACKES WEST AND CsH,02NpB~3 U i b r o n i o m a l o ~ i b r c ~ m o p l i e n y l a t n i d e (EACKES WEST and CBHsONCl Oxiine of 6-chloro-l-hydrinIlolle (KEWER and WITHAM) 1461.C,H,O,N,Br, 9 I V WHITELEY) 373. WIIITELEY) 373. B r o 111 o in a 1 o 11 b I' o 111 o p h e n y 1 a m i d e ( BACKES WEST and WHITELEY) 373. M a l o n d i b r o m o p h e n y l a i n i d e ( RACKES Wwr and WHITELNY) 373. CBH,0,N,S2 D i t h i o m e s o x om o n op h e n y l a In i d e (NAIR) 1237. C,H,O,NCl E t h y 1 2-c h loro-3-11 i t r o be11 z o a t e ( KENNICEL aild ST~JBBINGS) 598. E t h y l c h l o r o n i t r o b e n z o n t e s conder~sation of with hydrttzines (KENSER and WITHAM) 1053. C,HsO,NI E t h y l 2-iodo-3-nitrobenzoate ( K m s r m and Smimws) 699. C,H,O,N,Br 2:4-Di n i t r o p h e n y 1 87-d i b r o m opropy 1 e t 11 e r ( FAIRBOURNE C,H,O,N,Cl 2-C h l o ro-3:li-d i n i t r oa c e t o-p-t 01 u i d i d e (DAVIES) 868.CoHoO,N,C1 F o r m a t c of 5-c h l o r o-6-ni e t h y 1 be n z i m i n a z o l e (MORGAN and CHALLENOR) 1542. C,H,,ON,S w-Ami n o a c e t o p h enon e t h i o c y a n a t e (GBANT and PYMAN) 1896. CBH1102NS 8-Hy d r ox y e t h y 1 p h e n y 1 t h i o c a r bnm a t e (RENNIwr and WHIN-C,Hl,O,NT1 T h a 11 i u m d i m e t h y 1 3-11 i tro-o- t o 1 y 1 o x i cie (GODDAI:D) 1311. COH,,O6N,Br ~ r o m o m a l o n y ~ d i u r a t h a n e (BACKES WEST and WIIITELET), 372. C,H,,O,N,Br D i bromomalondi-n-pr o p y l a m i d e (BACKES WEST and WHITELEY) 368. CDHI7O2NeBr Broniom alondi-n-propylamide (RACKES WEST a n d W H I T m m ) , 367. C,H2t0,N,Co cisCi t r a c o n a t o d i e t h y l e n e d i a m i n e c ob a1 t i c h y d r o x i d e , hydrogen citraconate of (DUFF) 389.and TOMS) 1038. COP) 1661. Clo Group. CloH12 T e t r a h y d r o n a p h t h a l e n e preparation of derivatives of (KON and CloHl H y d r o c a r b o n from Andropogon Jwarnnczwx (SIMONSEN) 3649. 10 I1 C,,H,O, CloH,N CIoHloO C,,H,oO 6-Hydro x y-5-car boxy-m-t o l y l a c e t ic acid and its silver salt 3-Methoxy-4-methyl-o-phthalic a c i d and its salts (SIrdoNsEx and RAU), m-Opianic acid and its silver salt (FARGHER and PEKKIN) 1739. STEVENSON) 87. 3-M e t h o x y-4-me t h y 1-o-p h t h a li c a n h y d r i d e ( SIMOWSEN and RAU), Q u i n a l d i n e synthesis of (MILLS HARMS and LAMBOURNE) 1294. a r - D i h y d r o - a - n a p h t h o l s (ROWE and LEVIN) 2021.1344. (ALIMCHANDAXI and MELDRUM) 209. 1345. CloHroN2 Cl,Hl,C1 CloHlaO, 6-A m i no y u i n s l d i n e (HAMER) 1435. 4 - C h l o r o b u t e n y l b e n z e n e (MORGAN and HICKIKBOTTOXI) 1886. n- and iso-Eugenols analysis of mixtures of (McKIE) 777. H y d r o x y p h en y 1 n-pr o p y 1 k e t o n e s (MORGAN and HICKINBOTTOM) 1884. 216 FORMULA INDEX. 10 11-10 111 CloH1203 5-H y d r o x y-4-ni e t h o x y-o- t o 1 y 1 xri e t h y 1 k e t on e (FANGHER and PERKIN) 1733. C1,HI2O E t h y 1 6-e thoxy-2-pyrone-5-carl-,ox y 1 a t e (INGOLD and PEKREN), 1601. C,oHlzN2 cydoW exan e spirocyclop r o pa n e-2 :3-di c a r b o x y 1 on i t r i 1 e (BIRCH, 1 4-cndoM e t 11 y 1 e ne-6-me t h y 1 t e t r a h y d r o q u i n ox a 1 i n e and its salts ( AlooRE GOUGH and IIoN) 1328.and DOUBLEDAY) 1172. YURNER) 430. Cl0H&1 4-Cliloro-n-butylbenzene (MORGAN and HICKINBOTTOM) 1886. Cl0H ,AS As-Methyltetrahydroarsinoline and its salts (BURROWS and C,,H,,O ycZoPen t a n espirocyclohexane-3:5-dione (NORRIS and THORPE) 1207. c,0H?fo3 H y ti r o x y k e t o d i h y d r o c pic a m p ho 1 e n i c ( PERKIH and C,,H,,O Benzoyl g l y c e r i d e (FAIRBOURNE and Toxrs) 1040. 1 a c t o n e 1 ITLEY) 1106. y-L a c tone of l - h y d r o xy cyclo h ex y l e t h a n e-aB-d i c a r b o x y 1 i c a c id and its silver salt (BIRCH GOTJGH and KON) 1326. CloHl,N E p i c amp 11 o 1 en o n i t r i 1 e (PERKIX and TITLEY) 1102. CloHleO Epicamplior (PERKIN and TITLEY) 1089. cycEoH e p t e n y lace t on e (KoN) 827. Piperitone (READ and SniITH) 779 ; constitution of (SIMONSEN) 1650.Epicampholenic a c i d s (PERKIN and TITLEY) 1103. C,,H1,O D i h y d r o epi camp h o 1 en o l a c t o n e (PEKKIN and TITLEY) 1104. C1,H,,O l - H y d r o xy cyclo h e x y 1 e t h a n e-ab-d i car l~ ox y l i c silver CloHl,C1 Hydro c h 1 o r id e of hydro c a r b o n C,,II, (SIMONSEN) 1649. C1oHlaBrs CloH,,N E-Epicamphylamine (PEKKIN and TITLEY) 1105. CloH,,O Trim e t h y l-B-m e t h y l gluc o si de (IRVINE and OLDHAM) 1758. acid salt (BIRCH GOUGH and KoN) 1327. D i hydro b r om i d e of h y d r o c a r b on CloHl (SIMONSEN) 1650. 10 I11 CloH,02N 1:2-N a p h t h a qu i n on eLl-oxime hexamminocobaltic salt (MORGAN and SMITH) 708. CloH60sN 7-0xy-1:2-naphthaquinone-l-oxime pentamminodicobaltic salt (MORGAN and SMITH) 709.C,,H,ONa Sodium-B-naphthoxide velocity of reaction of ethyl iodide and (Cox) 149. CloH,03N 7-H y d r o x y-1:2-n a p h t h a q u i n one-l-ox i me cobaltic salt (MORGAN and SMITH) 705. Cl,HiBr,Bi a-Naph t h y l d i b r o m o b i s n i u t h i u e (CHALLPNGER and ALLPRESS), 919. C,oH,OzS CloH80,N4 D i n i tro-2 3:6:7-d in] e:t h y l e n e t e t r a o x y an t h r aqu i II one di-imi de C1oH,O,N 2:4-Di n i t r o-5:s-d i h ydro-a-naph t h o 1 ( ROWE and LEVIN) 2028. CloH902N Scatole-2-carboxylic a c i d (KERYACK PERKIN and ROBINSON), 1634. CloHgOsN 2-Methoxy-3-cyano-p-tolui c acid and its silver salt (SIMONSEN and RAW) 1344. 6-M e t h o x yin do1 e-a-car b ox y 1 i c a c i d ( KERMACK PERKIN and ROBINSON), 1632. 3-M e t h oxy-4-m e t h y l-o-ph t h a l i m i d e (SIMONSEN and RAU) 1345.N i t r o d i h y d r o-a-n a p h t h o Is ( ROWE and LEVIN) 2026. 2-A c e t y l-$-ox y(1)t h i ona p h t h e n (SMILES and MCCLELCAND) 1814. ( KEFFLER) 1479. CloH,O,C1 m-Chl o r o be nz y l m a1 o n i c a c i d ( KENNER and WImAhI) 1460. 216 10 I11 FORMULA INDEX. CloH,OsN o-N i t r o-pm e t h o x y p hen y 1 p y r 11 vi c a c i d (KERMACR PERKIN and C,0H1003C12 4-H y drox y -5-Bp-d i c h 1 o roe t h y 1-21%-t o l u i c acid and its calcium C ,H1,0,N2 2:3 :6:7-D im e t h y 1 e n e t e t r a o x y an t h r a q u i n o n e d i-im i d e (KEF-C,,Hl0O,Br a:5-D i b r o m o-8-h y d r o x y-2-m e t h o x y-fl-ph e n y l p r o p i onic ac i d , C1,HllON 6-Methoxy-3-me t h y l i n d o l e (KERMACK PERIEIN and ROBINSON) C,,H,,OCl Chlorophenyl n-propyl k e t o n e s (MORGAN and HICKINBOTTOM), C1,H,,O,N 3-Methox y-4-e t h o x y benzoni t ri l e ( KRFFLER) 1481.CloH,,O,N N i t r o p h e n y l 12-propyl k e t o n e s (b1oRC)AN and HICKINBOTTOM), CloH,,O,N 3-N i t r o-4-h y d r o x y p h e n y 1 n-pr opy 1 k e t o n e (MORGAN and CloHllO,N 4-C a r b e t hox ya m ino-m-h y d rox y b e m o ic a c i d ( FROELICHER and CloHllClBr2 4-Chloro-US-dibromo-n-butyl benzene (MORGAN and HICKIN-C,oH,20zBr2 cycloPen t a n espiro-4:4-di b r omocydoh e x ane-3:5-dione (NORRIS Cl,H120zS cycZoP en t a n e spiro-3:5-di k e t o-4-di t h i o cgclo h e x a n e (NAIK) 1240. CloH1204N A c e t y l derivative of 3-ni tro-2-methoxy-p-toluidine (SIMONSEN Cl0Hl2O4N4 Ace t o n e d i n i t ro t o l y l h y d r azon es (BRADY and BOWMAN) 899.n-Pr op a1 d e h y d e-2:4-d i n i t r o-m-t 01 y 1 h y d r a z on e (RRADY and BOWMAN) 899. C,,H,,ON Arninophenyl n-propyl ketones and their salts (MORGAN and C,,H,,O,Br eyclo P e n t a n e qi,iro-4-b ro in ocycloh e x a n e-3:5-di o n e (NORRIS and CloH,,O,N 4-Diazoamino-3:5-dim e t h y l isooxazole (MORGAN and BURGESS), CloHl,O,N 35-D i m e t h y 1 is0 o x a zo 1 e-4-a z 0-a c e t y 1 acetone and CloHl,0N2 Ace t y 1- 4:6-d i a m i n o-nz-x y l e n e (PEARMAN) 718. CloHl,CIAs y-P h e n y 1 prop y l m e t h y l c h l o roar s i ne (BURROWS and TURNER), 430. C,,H,,BrAs y-P h e n y l p r o p y lm e t h y 1 br o m o ar s i ne (BURROWS and TURNER), 430. CloHl,04N E t h y 1 a-c yanopropane-By-dicar b ox y l a t e (INGOLD) 340.CloHlsO~NP 3-N i t ro p h en y 1 12-p r o p y 1 k e t o n e p-n i t r o p h e n yl h y d r B z o n e CloHlsOIBrs E t h y 1 di b r o m oa d i p a t e s (INGOLD) 962. C10Hld041B E t h y l di-i odba d i p a t e s (INGOLD) 963. Cl,Hl,ON Piperitoneoximes (READ and SMITH) 784 ; (SIMONSEN) 1651. Cl,Hl,OAs Phenyldimethylethylarsonium hydroxide saltsof ( B u ~ ~ o w s C1,Hl,OzC1 Pinene chloroliydrins (HENDERSON and MARSH) 1497. C1,H1,O4C1 E t h y l a-chloroadipate (INGOLD) 961. C10H1,04Br E t h y l a-bromoa d i p a t e ( INGOLD) 961. CloH~s02Clz or ROBINSON) 1630. salt (ALIMCHANDANI and MELDRUM) 208. BLER) 1479. and its brucine salt (READ and ANDREWS) 1783. 1640. 1885. 1883. HI CKINDOTTOM) 188 8. COHEN) 1430. BOTTOM) 1887. and THORPE) 1210. and RAU) 1342.HICKINBOTTOM) 1883. THORPE) 1210. 1547. BUKGESS) 1546. (MORGAN ( NORGAN and HICKINBOTTOM) 1882. and TURNER) 1450. 1:2-D i ch lor0 m e n t h a n e-6:8-d i o 1, Pinene d i c h l o r o h y d r i n s (HENDERSON and MARSH) 1495. S o b r e r ol dio h l o r i de (HENDERSON and MARSH) 1496. 216 FORMULA INDEX. 10 111-11 I1 C,,H2,OaNa CloHBION dt-Pip e r i t on e h y d r ox yla m i n o-ox i ni e (READ and SMITH) 783. l-isoButoxymethylpiperidine preparation of (MCLEOD and ROBIN-SON) 1474. 10 IV Cl,H,OoNS 8-0xy-1:2-n a p h t haquinon e-2-oxime-3:6-disu I p h onic acid, C,,H70,NS 1:2-N a p h t h a q u i no ne-2-0 x i m e-4-53 u 1 p hon i c a c id,. cobaltic and CloH,09NSa 8-Hydr oxy-l:2-n a p h t ha q u i n on e-2-0 xim e-3:6-disul p h o n i c CloHoOaNzI 6-N i t r o q u i n o l i n e m e t h i o d i d e ( HAMER) 1435.C,,H,,ON,Cl C h l o r o-l-h y d r i n done C,,H,,O,N,S D i thiom e s o x o m o na-p-t o l u i d i d e (NAIE) 1237. CloHlo08Nc1 4-0 h l o r o-3-ni t r op h e xy 1 n-prop y 1 k e t o n e (MORGAN and C,,H,,ONCl 4-Chloro-3-aminophenyl n-propyl ketone and its hydro-CloH1202N8Br 5-B r om o-2-m e t h ox y p h en y 1 acetaldehyde semi c a r b a z on e CloH120,N8T1 T h a l l i u m d i e t h y 1 2 4:6-tr i n it rop h en ox id e (GODDARD) 1313. Cl,H180,N,T1 T h a l l i u m die t h y 1 2:4-di n i t r op he n o x i d e (GODDARD) 1313. C,,H,,O,NTl T h a l l i u m d i e t h y 1 n i t r o p h e n o x i des (GODDARD) 1312. C,,Hl,05N8T1 T h a1 1 iu m d ie t h y 1 (GOD-C,,H,,ONBr Dibromopiperitoneoxime (SIMONSEN) 1652, CloH1,0N21 Substance from eseroline methiodide methyl iodide and sodium pentamminocobaltic salts ( MOEGAN and SMITE) 713.8-naphthylamine salts (MORGAN and SYI'PH) 710. acid cobaltic and B-naphthylamine salts (MORGAN and SMITE) 713. s e m i c a r b a zo n e s (KENNER and WITHAM) 1459. HICKINBOTTOM) 1887. chloride (MORGAN and HICKINBOTTOIM) 1888. (READ and ANDBEWS) 1785. 4:6-d i n i t r o-2-am i n o p he noxide DARI)) 1313. ethoxide (STEDMAN) 892. 10 VI CloH2,07N.,BrSaCo cis-Br o m o b en z en e-3:4-disulphon a t o d i e t h y 1 e n e d i-amineco b a l t i c hydroxide salts of (DUFF) 1986. CI1 Group. C1,H,Os D i h y drox y n ap h t h a Id e h y d e s (MORGAN and VINIXG) 177. C11H804 Substance from sodium and phenyl acetate (PERKIN) 1289.CllH8Ns Norharman and its salts (KEBMACK PZRKIN and ROBIXSON) 1602. CllHl,,O 4:5-Dimethoxy-o-phthalonic a c i d (-I- 2Ha0) aud its acid calcium C,,HI20 o-Methoxystyryl m e t h y l k e t o n e (HEILBRON and BUCK) 1509. C,,Hl,O M e t h y l m-opianatcs (FARGEER and PERKIN) 1741. CllH1402 dZ-trans-cycZoPentane-l:3-~iicarboxyl i c acid resolution of (PERKIN and SCARBOROUGH) 1400. Cl,Hl,O E t h y 1 6-e t h oxy-3-m e t h y l-2-p y ron e-5-carb ox y l a t B (INGOLD and PERBEN) 1601. C,,H,,O Lac t o n e of l-h y d ro x y cyclo hex y 1 e t h a n e-a&?-t r i c a r b oxy li c a c i d (BIRCH GOUGH and KoN) 1326. Cl,H,,N 1:4-endoE t h y l e n e-6-me t h y 1 t e t r a h y d r o qu ino x a l i 11 e and its salts (MOORE and DOUBLEDAY) 1174. CllHlsOa H y dr ox y me t h y l e n e-Z-e p i c am p h or (PERKIN and THORPE) 1096.CllHle04 cycZoH exan espi?"ocycZo hexa ne-3:5-d ion e (NoRRIs and THORPE) 1205. CllHleOI E t h y l cyclopentanonedicarboxylate (INGOLD) 349 ; (INGOLD and CllH1707 1 -H y d r ox y cyclo h e x y l e t h ane-aSB-t 1 i c a r b o x y 1 i c acid silver salt salt (FARGHER and PERKIN) 1735. TKORPE) 499. (BIRCH GOUGH and KoN) 1326. CXIX. 2169 4 il 11-11 111 FORMULA INDEX. C,,H,,As y-P h e n y l p r o p y 1 dime t 11 y l a r s i n e (BURROWS and TUENEI~) 429. C,,H,,O E t h y l t r i m e t h y l sacchnrolactone (IRVINE and OLDHAM) 1757. 11 I11 CllH,03N 2-C arbox y i n d o 1 e-3-a c e t i c a n h y d r i d e (I~ERMACK PERKIN aud C11H,04N 1 :2-N a p h t ha q u i n o 11 e-1-0 x i m e-3-c a r b ox y 1 i c acid cobaltic salts CllH,OsN 2-m-Ni t rop h en y l g l y oxal ine-4:5-dicar box y l i c acid (FARGHER), C,,HsON 5-K e t o-4:5-d i h y d r o i n d o 1 e d i a z ine(l:4) (KERMACK PERKIN and Cl1H8O2NZ Norharmol (KERM~cK PERKIN and ROBIMOK) 1619.C11Hs03S C11H,04N 2-Carboxyindole-3-ace t i c acid (KERMACIC PERKIN and ROBIN-C11Hg04N3 2-m-Aminop h e n ylglyoxaline-4:5-dicar box y 1 i c acid (FAR-C11Hlo03N2 2-Carb o x y i n do1 e-3-ac e t a m i d e ( KERMACK PERKIN and ROBIN-CllHloOsNI 5-Ni t r o - p a c e t y lam inophen y l g l y o x a l i n e (GRANT and PYMAN), Cl,H,,O,N Dime t h y 1 d i k e t o t e t r a h y d r o q u i n a z o l i n e carbo x y li c a c i d CllHllOzN 1 :3-D i m e t h y 1 i n d o le-2-c a r b o x y 1 i c a c i d ( KERMACK PERKIN and 3-Methoxy-4-methyl-a-quinolone (KERMACK PERKIN and ROBISSON) 1635.CllH110,N3 1-p-N i t r op h e n y 1-3:5-di m e t h y l p y r azol e (MORGAN and DREW), 621. CllHl103N 6-11 e t h o x y-3-n1 e t h y 1 i n d ole-2-c arb o x y l i c acid ( KERMACK, YERKIN and ROBINSON) 1640. CllH110,N3 3:5-D im e t h y 1 is0 ox a z ole-4-az o r es or c i n 01 (MORGAN and BUR-GESS) 703. CllHlzOsWr cycZoH e x a n espiro-2:3-di c y an o cydo p r op a n e-2-c ar b o x y 1 i c a c i d (BIRCH GOUGH and KoN) 1325. CllHla03NZ Acetylacetone-p-nitroanil (MORGAN and DREW) 624. CllH1304N2 l-p-N i t r oa n il i n o ace t y lace t o ne (MORGAN and DREW) 623. CllH130N cycloH ex a n e spiro-2:3-d i cyan ocyclo p r o p a n e-2-c a r bo x y 1 amid e Cl,H1304N o-Methoxystyrylmethyl ketoxime (HEILBRON and BUCK) 1509.CllH1301N Car b e t h o x y aini no-m-m e t 11 ox y b e n z o i c acids (FROELICHER and CllH1306N3 Ace t y 1 derivative of 4-n i t r o-2-car be t h o x y p h e n y 1 h y d r azi ne Cl,H140eN2 M e t h y l m a l on om o u o-o- t o l u i d i d e (NAIK) 1238. CllH140,C1 cycEoH exan e.spiro-4:4-di c h 1 o r o eyclclo h e x a ne-3:5-d i one Cl1Hl4O2Br2 cyycZoHe x a n espiro-4:4-di b r o m ocgclo h exan e-3:5-di o n e CllH1404N4 a-R u t a 1 de h y d e-2:4-di n i t ro-m-t 01 y l h y d r az on e ROBINSON) 16'23. (MORGAN and SMITH) 709. 163. ROBINSON) 1627. (1)T h i o nap h t h a-4-0 x y c o u in a r i n (SMILES and McCLELLAND) 1815. SON) 16122. OHER) 163. SON) 1623. 1902. (SCOTT and COHEN) 668. ROBINSON) 1636. (BIRCH OOUGH and KoN) 1324. COHEN) 1431.( KENNER and WITHAMI 1055. (NORRIS ( NORILIS (BR~DY and Met h y 1 e t h y 1 k e t o n e 2:4-d i n i t r o-m-t o 1 y 1 h y d r a zo n e (BRADY and Bow-CllH1502C1 cycZoH ex anespiro-4-c h l o P ocyclo h ex ane-3:5-dio n e (NORRIS and and THORPE) 1209. and THORPE) 1209. ROWMAN) 899. BlIC.N) 899. THORPE) 1209. 217 FORMULA INDEX. 11 111-12 I1 Cl1Hl5O8Br cycZoH ex a n espiro-4-b r o m o cyc20 h e x a n e-3:5-d ion e ( NORRIS and C,,H150,N 4:5-Dimethoxy-o-tolyl m e t h y l ketoxime (FARGHER and PER-CllH150sNs 5-H y d r o xy-4-m e t h o x y-o-t 01 y l met h y 1 k e t o n e 8 em ic a r ba z one C11H1501N E t h y 1 a-cy an o-7-m e t h y I g l u t ac on a t e (INGOLD and PERREN), Cl1HlsIAs As-Me t h y l t e t r a h y d r o a r s i n o l i lie m e t h i o d i d e (BURROWS and Cl1H1,ON A mino met h ylene-e p i cam p h o r (PERRIN and TITLEY) 1101.Cl1H1,0,N E t h y l c y a n o m e t h y l g l u t a r a t e s (INGOLD) 338 ; (INGOLD and CI1H1,0,N3 Semicarhazone of acid C,,H160, from oxidation of E-epicnmpho-Cl1Hl8O4Br2 CllHIDONS cycZoH e p t e n y l a c e t n 1 1 e se in i c ar bazo n e (KoN) 827. C,lH2202N2 Malondi-n- and -iso-butylamides (BACKES WEST and WHITELEY), 368. Cl1H,O6N2C1 acid ( f 2H20) (MORGAN and CHALLENOR) 1540. C1,H,O,NpBr 2-p-Bromobenzeneazoglyoxaline-4:5-dicarboxylic a c i d (FAROHER) 162. C,,H,O,N,Br 4-p-Bromo b enzeneaz o-2-me t h y 1 g l y oxal i n e-5-car boxy l i c acid (PARGHER) 161. C,,H,O,N,Br 2-p-Brom o b e 11 z e n e h y d r a z o gl yo xa 1 i n e-4 5-di c a r b o xy 1 i c acid (FARGHER) 163.C,,Hl,OaNaBr p-B r o in o be n z e ne a z o a c e t y l ace t o n e (MORGAN and DREW), 622. C1,HllO,N,I 6-Ni t r o q u i n a l d i ne m e t h i o d i d e (HAMPR) 1435. C,,H,,O,ClBr cycZoH e xa n espiro-4-c h 1 or o-4-b rom ocgclo-h e x a n e -3:5-di o ne CllHIG03NT1 T ha1 l i n m d i e t h gl n i t r o t ol yl o x ides (GODDARD) 1314. C11H2,0aN2Bra D i b r om o ma1 o n d iiso bu t y 1 amid e ( BACKES WEST and THORPE) 1208. KIN) 1732. (FARGER and PERKIN) 1733. 1597. TURNER) 431. THO WE) 500. lenic acid (PERKIN and TITLET) 1107. isoPr op y 1 ad-d i br om ogl 11 t a r a t e ( IKGOLI)) 318. P i p e r i t o n e seniicnrbazones (READ and SMITH) 784 ; (SIMONSEK) 1650. 11 IV 6(7)-Ch 1 o r o-f(6)-me t h y 1 q u i n o x a l i ne-2:3-d i ca r b ox y 1 i c (NORRIS and THORPE) 1210.WHITELEY) 370. CllH2102N,B~ B rom o ma1 ond i-n- and -.iso-bu t y 1 a m ide s (BACKES WEST and WHITELEY) 368. 11 v CllH210eN6SC~ cis-o-S u l p 11 o be n zo a c e t a t o d i e t 11 y 1 e n e d i an1 i n e c o b a1 t i c h y d r o x i d e salts of (DUFF) 1985. 11 VI C,,H2,0,NdBrSCo cis-o-S u 1 p h ob e n z oac e t a t o d i e t 11 y 1 e n e d i am i n c c o ba 1 t i c bromide (+ H,O) (DUFF) 1985. Clz Group. Cl2HoN Carbazole oxidation of (PERLIN and TUCKER) 216 ; additive vompound of 4’-dimethylamino-2-l~ydroxydistyrylketone with ( HEILBRON and BUCK), 1512. C,,H,,N Harmine (KERMACK PERKIN and ROBINSON) 1602, Cl,H,,N 6 - E t h y l q u i n a l d i n e (MILLS HARRIS aud LAMBOURNE) 1300. Te trahydrocarbazole and its picrate (PEILKIN and PLAKT) 1831.217 12 11-12 111 FORMULA INDEX. ClrHl,O Ace t y 1 derivative of 5-h y d r o x y-4-m e t h o x y-o-t 01 y 1 m e t h y 1 k e tone C,21i1,Nr 6-Amin o t e t r a h y d r o c a r b az o 1 e (PERRIN and PLANT) 1833. CL2HlsN2 1 :4-endo T r i m e t h y 1 en e-6-m e t h y 1 t e t r a h y d r o q u i n o x a l i n e and its C12HlaOB E t h y l a c o n i t a t e preparation of (INGOLD) 350. ClaHz,,Oa E t h y l a-acetoxyadipate (INGOLD) 966. C12Ha2011 Cellobiose constitution of (KAWORTH and HIRST) 193. (FARGHER and PERKIN) 1733. salts (MOORE and DOUBLEDAY) 1174. 12 I11 CIaH&12& S u b e t a n ce from chlorobenzene and sulphur chloride (RAY) 1963. Cr2He03N2 Norharmolcarboxylic acid and its sulphate (KERMACK PERKIN, and ROBIN~ON) 1618.C,2He0,C1u. 6-M e thyl-2:4-bi s t r i c hlorome t h yl-l:3-benzdioxin e-8-c arbo xy-l i c acid and its sodium salt (ALIMCRANDAKI and MELDRUM) 208. C12HloON2 5-Ke t o-7-me t h y 1-4:5-d i h y d r o i n d o 1 e d i a z i n e (1:4) (KERNACIC, YERKIN and ROBINSON) 1635. 2-Ke t o-l-me thyl-2:3-d i hydro norharman (KERMACK PERKIN and ROBIN-SON) 1638. CIPHloOZNI l l - M e t hoxy-5-ke t o-45-dill y d roind ole d i a z i n e ( 1:4) (KERMbcK, PERKIN and ROBIXSON) 1633. C,,Hl0OaN2 cyc20 H e xa n espiro-2:3-d i cyan Q cyelopr o pa n e-2:3-d i c a r box y li c a n h y d r i d e (BIRCH GOUGE and KoN) 1328. C12HloN2S2 D iam i n o t h i a n t h r e n (RAY) 1964. C,2Hl10,N 4-N i t ro be n z y 1 i d ene ami n o-3:5-di me t h y l isoox a z o 1 e s (MORGAN C,,HIlO,N 6-M e t h o xy-2-c a r bo x y i n d o 1 e-3-ace t i c a c i d (KERbrAcK PERKIN, C12H120Ns Ace t y l am i n o q u i n a l d i n e s ( HAMER) 1438.and BURGESS) 701. and ROBINXON) 1641. 4-B en z y 1 i d e n e a m i n 0-3 :5-d i m e t h y 1 iso o x a z o 1 e (MORGAN and BURGZSS), C,2H1202N2 4-B enzo y 1 ami n 0-3:5-dime t h y 1 is0 oxaz o 1 e (MORGAN and BTJR-C12Hl,0sN4 4-p-N i t r o b e n zy 1 i d e n e h y cl r a z i n 0-3:5-dim e t h y l isoox az 01 e ClrHlZO4Ng cyclo H ex a n e spiro-2:3-d i c y a n o q c l o pro p a n e-2:s-d i c a r b o x y 1 i c Me t h y 1 dim e t h y l d i k e t o t e t r a h y d r o q u i n az o l i n e c a r b o x yl a t e (SCOTT C12H1802N E t h y 1 a-k e t o-8-o-n i t r o p h en y l b u t y r a t e (KERMACK PERKIN and ClaHlaOgN cyclo H ex a n e spivo-2-c y a n o cyclopr o p a n e-2:3:3-t r i c a r b o x y 1 ic ClzH1,ONo A c e t y 1 derivative from base C,H,,N (PEARMAN) 720.C,,H,,O,N 2:6-Dinitro-m-4-xylyl n-propyl k e t o a e (MORGAN and HICKIN-701. GESS) 701. (MORGAN and BURGESS) 1548. acid (BIRCH GOUGH and KoN) 1327. and COHEN) 669. HORINSON) 1634. a c i d (BIRCH GOUGH and KoN) 1328. BOTTOM) 1891. C12H160Cl 6-Chloro-m-4-xy'lyl n-pr o p y l k e t o n e (MORGAN and HICKIN-ClZHl6O2N 3-Acetylaminophenyl n-propyl k e t o n e (MORGAN and HICKIN-C12H160aN N i t r o-m-4-x yl y1 n-prop y 1 k e t o n e s (MORGAN and HICKINBOTTOM), BOTTOM) 1891. BOTTOM) 1883. 1890. C,H,,OW 6-Aminom-4-xylyl n-propyl ketone and its salts (MORGAN and HICKINBOTTOM) 1890. 217 12 111-13 I FORMULA INDEX. C12H170,NI 2:4-D i n i t ro-B-d i e t h y ! am i n o e t h y 1 b e n z en e and its salts (Mc-C,,H,,O,N H y d r o x y m e t h y l e n e-e p i cam p h o rse m ica r baz on e (PICRKIN and C,,H,,O,N S em icarbaz o n e of e t h y 1 cyclo 1) en t a n on e-2:4-di car b ox y 1 a t e Cl,H,OeNP E t h y 1 ad-d i c arbam y l-p-m e t h y 1 g l u t a r a t e (GUPTA) 304.C,,H,,IAs y-P h e n y l p r op y 1 d i ni e t h p 1 a r s i n e In e t h i o d i d e (BURROWS and CI2H2,O,S D i a c e t y 1 derivative of s u l p hi d obi s-B-h y dro x y di e t h y 1 su 1 p h-LEOD and ROBINSON) 1476. TITLEY) 1099. (INGOLD and THORPE) 500. TURNER) 429. i d e (BENNETT and WHINCOP) 1863. C,,H,,O,N E t h y 1 C12H2,0,N Pi peri t o n e h y d rox y 1 ami n 0-ox ime s ( SIMONSEN) 1651. I-7-2 c e t y 1-a.is0 p r o p y 1 b u t y r a t e semi car b az o n e (SI-MONSEN) 1653. 12 IV C12H60,C1,S Substance from oxidation of dichlorothianthren (RAY) 1962. C&06N2Ba Barium n i t r o p h e n o x i d e s ( GODDARD) 1162. C12HB06N2Ca Ca 1 ciu In n i t r o p h en o x i d e s (GODDARD) 1164. C12H,0,N2Sr S t r o n t i u m n i t r o p h e n o x i d es (GODDARD) 1163. CIIHloO,NeS 6-Ac e t y l a m i n o-1:2-na p h t h a q u i no n e-2-0 xi me-3-sul p honicr acid cobaltic and B-naphthylamine salts (MORGAN and SMITH) 711. CI2Hl,O,N,C1 8-C h l o r o-5-n i t r o t e t r a 12 y d r o c a r bazol e (PERKIN and PLANT), 1837. C12Hl,0,N,S 8-A ce t y lam i n 0-1 :2-n a p h t h aq u i n on e-2-oxim e-3:6-di s u l p h -onic acid pentamminocobaltic salt ( NORGAN and SMITH) 712. C,,H,,O,NCl E t h y l 7-c hI o ro-1-i m i n o h y d r i n d e u e-2-car b ox y l a t e ( KENNER and WITHAM) 1459.C,,H,,O,Cl,Te Tell u r ium 0-e t h y 1 be n z o y 1 acetone t r i c h l o r i d e (MORGAN Cl2H1,OsNS2 Cl4H1,O2NSC1 cyclo H e xan on e-2-c h l o ro-5-n i t r o p h e n y 1 h y d rax o n e (PEI~KLN C12H,,0,N,Co cis-” 11 t ha l a t o d i e t h y 1 en e diarnin e co b a 1 t i c h y d r ox id e salts Cl2H,,O4N,Sn M e thy 1 in a1 o n o d i m e t h y 1 a m i d e cl i s u 1 p h i d e (NAIK) 1239. C12H1204N,SAs2 C12Hl,0,N2SAs, C,,H120,N2S2As4 C12H120,N,S2A~4 C12H1208NpStA~2 CI2H,,O,N,BrCo and DI~EW) 618. E t h y 1 d i t h io me s o x o t o 1 y l ama t e s (NAIK) 1237. and PLANT) 1837. of (DUFF) 1984. 12 v 3:3’-Diam ino-4:4’-di h y d r o x y-5-sulphin o arseno benz ene, 3:3’-D i a m i no-4 :4’-d i h y d r o x y-5-s u 1 p h oars e no b e n z e n e, 3:3’-Diam i n o-4:4’-di h y d r o x y-5:5’-disulp h i no a r ~ e n o -3:3‘-Diamino-4:4’-di h y d r o x y-5-sul p h 0-5‘~sul phino-3:3’-D i a mi n 0-4 :4’-d i h y (1 r o x y-5 5’-di s u l p h o a r s en0 be n hydrochloride of (KING) 1115.hydrochloride of (KING) 1117. benzene (KING) 1113. arsenobenzene (KING) 1118. e n e (KING) 1116. (+ 3H20) (DUFF) 1984. cis-P h t h a l a t o d i e t h y l e n e d iam i nec o b a1 t i c b r om id e C, Group. CIIHla FI norene additive compounds of 4’-dimethylamino-2-hydroxydist;yryl ketone with (HEILBRON and BUCK) 1511. 217 13 11-1s IV FORMULA INDEX. 13 I1 CisH1oO Cl,H,O3 CI3Hl5N ClsHlaN2 ClsH,,O, CIsHlaO, Ben z op he n one additive compounds of 4'-dimethylamino-2-hgdroxy-ac-1-K e t o-3-me t 11 y 1 t e t r a h y dr o n a p h t h y I-3-a cot i c acid and its distyryl ketone with (HEILBRON and BUCK) 1513.silver salt (KON and STEVENSON) 90. 9-Ede t h y l t e t r a h y droc a r b a z 01 e (PERKIN and PLANT) 1834. 6-Amin o-9-m e t h y I t e t r a h y d r o c a r kazo Ic and its picrate (PERKIN cyclo p e n t a n e spirocyclo h e x a n e-3:5-d io n e-2-c a r b o x y l a t e 1-He to-3-me t h y l oc t a h yd r o n a p h t h yl-3-ac e t i c acid and its silver and PLANT) 1835. (+ H20) (NORRIS and THORPE) 1207. salt (KON and STEVENSON) 92. Lac t o n e of 7:8-d i 11 y d r o xy-3:4-b i s t; r i c 11 1 o ro me t h y 1-6-8- t r i-(ALIM-ClsH,0sN3 N i t ro-3-k e to-2-p lie n y 1-1:3-di 11 y cl r o i n d azo 1 es and their sodium ClsH,O5N p-N i t ro b enzald oxi m e-AT-p-n i t r o p hen y 1 e t he P (BARROW and C1,H,,O,N Ace t y l derivative of 2-car box y i nd ole-3-ace t i m i d o (KERMACK, E t h y 1 13 111 ClaH6O6CI9 c h lo ro-a-h y d r ox ye t h y 1-1 :3-be n zdi ox i n e-5-c a r b a x y l i c n ci d CHANDANI and MELDRUM) 206.salts (KENNER and WITHAM) 1056. GRIFFITHS) 216. PERKIN and ROBINSON) 1624. p-Ni trobenzaldoxime-AT-phenyl e t h e r (BARROW and GRIFFLTHS) 213. 6-C hlor 0-3-p h en y 1-3:4-t oly 1 en edia z o i m i ne ClaH,oN3C1 (MORGAN and JONES) 191. C13Hl,04N Diinethyl2-carboxyindole-3-acetate (KERMACK PERKIN and HOBINSON) 1623. Cl,H,,N2Cl 6-C h l o r 0-3-11 he ny 1-3:4-to 1 y 1 e ne d i am i n e (MORGAN and JONES), 191.CISHIJNPCl R e n z en e-5-azo-6-c h 1 o r o-2:4-t o 1 y 1 en e d ia in i n e and its dihydro-chloride (MORGAN and JONES) 188. ClsHl,ON H a r m s l i n e (KERMACIC PERKIN a d ROBINSOX) 1602. ClSHl,02N8 6-Ni t ro-9-me t h yl t e t r a h y d r ocar bazo l e (PEEKIN and PLANT), C,,Hl,OsN D i a c e t 1 derivative of g l y c e r o l a-2:4-dinitrophenyl e t h e r C13H1,OsN E t li yl 6-m e t hox y-3-111 e t h y l i n dole-2-c a r b oxy la t e (KERMACK, C13Hl,0,N E t h y 1 a-ke t o-8-o-ni t ro-p-rn e t h o x y p h eny l b u t y r a t e ( KERMACIC, C,,H160,N2 hf e t 11 y l u t her of 4-p-h yd ro x y b eii z y 111 ydan toi n OG-di 111 e t h y l alsH,,O,N p - N i t r o a n i l i n o - e t h o x y a c e t o n e (MORGAN and DREW) 623. ClsHleNI 6-E t h y 1 q ui n a l d i n e met h i o d i d e (MILLS HARRIS and LAMBOURNE), 1800.Cl,H:,O,N E t h y l a-cyano-y-carbosyglntaconate and its metallic salts Cl,Hl,ON 8-D i e t h y lainin o p r op i o p h eno ne and its salts ( MCLEOD and Cl~H300zN2 Di (d i e t h y 1 amino ni e t 11 y 1) t I- im e t h y 1 en e c t h e r ( MCLEOD and 1834. ( FAIRBOURNE a n J Tom) 1037. PERKIN and ROBINSON) 1640. PERKIX siid l b E I s S O N ) 1639. e t h e r (Scorr and COHEN) 671. (INCOLD alld PERILEN) 1694. ROBINSON) 14 75. HOBINSON) 1473. 13 IV C,,H,O2N,C1 3-Chlor 0-5-n itro-2-phenylinclazole (KENNER and W r n r A n i ) , 2174 1057 FORMULA INDEX. 13 IV-14 111 C1,Hl,O,N,C1 C h 1 or o n i t r o p h e n y 1 t o 1 y 1 n i t ros oami nes and JOKES) 190. C,,H,,O,N,Cl C h 1 or oni t r o-N-p h e n y1 t olu i d i n es (MORGAN and JONES) 190 ; (MORGAN and GLOVER) 1704.C13Hl103NS E t h y l y-p he n y l c a r b am y l-ay-bi s d i s u l p h ido a c e t o a c e t a t e (NAIK) 1241. C1,Hl2O2N2S Benzene diaz o p t o 1 u e n e sii 1 p h i na t e (Dwr WHITEHEAD and WOHMALL) 2089. C13H1302N6C1 4’-N i t r o b e n ze ne-5-azo-6-c h 1 or o-2:4-t o 1 y 1 e ne d i am i n e (MOR-GAN and JONES) 188. C,,H,,ON,I Ace tylaminoquinal d i n e me t h i odid e s (HAMER) 1438. C,,Ha,ONBr u-Bromopropiono-d-bornylamide (SHIMOMURA and COHEN), 1822. Cl3H,,O5N,Co ch-H om o p h t h a l a t o d i e t h y 1 e n e d i a ni i n e c o b a l t i c h y d r o x-ide salts of (DUFF) 1986. (MORGAN 13 V CI,H,,O,N,SCo cis-Ben zy l s u l p h o ace t a t o d i e t h y 1 en e d i ami n eco b a1 t i c hydroxide salts of (DUFF) 1985.13 VI C1,H,O,N,BrSCo cis-B e n z y l s u l p h oac e t a t o d i e t h y 1 en e d i a m i ne c o bal t i c bromide (+ 3H,O) (DUFF) 1985. C14 Group. Cl4Hlo P h e n a n t h r e n e additive compound of 4’-dimethylamino-2-hydroxy-C,,H, 9:lO-D i h y d r o p h e n a n t h r e n e preparation of (HENSTOCK) 1461. C1,H2 1:4-D i-a-b u t y 1 be n z e n e (MORGAN and HICKINBOTTOM) 1892. 14 I1 C14HBOs E l l a g i c acid formation of from gallotannin (NIERENSTEIN SPIERS, distyryl ketone with (HEILBRON and BUCK) 1511. and GEAKE) 276. D i b r o m op h en a n t h r e n e (HENSTOCK) 57. Brom ophenanthrene dibromide (HENSTOCK) 57. l - H y d r o xy-3-me t h y l x a n t hon e and its potassium derivative (PEK-1291.I:lO-Dime t hyl-5:6-naph t h rtisod i a z i n e (KENRER and STUBBINGS), ac-l-Ke t o-3-e t h y 1 t e t r a 11 y d r o 11 a p h t h y 1-3-ac e t ic salt (KON and STEVENSON) 92. 6:6‘-Diamino-2:2’-ditolyl (KENNER and STUBBINGS) 600. acid and its C14H,l?N, C14Hm04 E t h y 1 C,,H,N 2-Amino-l:4-di-1~-butylbenzene and its salts (MORGAN and HICK-cyclo h ex an e spirocyclo h e x a n e-3:5-d i o n e-2-c a r b o x y l a t e (+H,O) (NORRIS and THORPE) 1204. INBOTTOM) 1892. 14 I11 CloHsOBp2 D i bro m o p h e n a n t h ron e (HENSTOCK) 58. C,H,O,N Dilactam of y-6:6’-diaminodiphenic a c i d (KENNER and STUB-C,,H,04Ss T h i an t h r e n d i c a r b ox y l i c acid (RAY) 1966. CllHSOBNl “ H y d r a z i d e ” of ?-6:6‘-dinitrodiphenic a c i d (KENNEE and CI4H8O9Na y-6:6’-Dinitrocliphenic acid and ite salts (KENNER and STUR-C,,H,O,N N i tro-l-hydroxy-3-m e t h y l x a r i t h ones (PERKIN) 1293.2175 BING~) 601. STUBBINCS) 600. BINQS) 593 14 III-14 IV FORMULA INDEX. C14B,NBr2 D i bromo-9-a m i n o p h en a n t h r e n e (HENSTOCK) 59. C,,H,,OCl Diphenylchloroacetyl chloride action of magnesium phenyl C14Hlo04S2 rrz-Dit hiobenzoic acid (SXILES and STEWART) 1792. C14H,,06N y-6:6’-D i n i t r o d i p hen am i d e (KEENER and SrumINGs) 599. C14H1,,0,S2 Benzoic a c i d m-disulphoxide (SMILES and STEWART) 1797. C14H,,N4S 4‘-Tri a z o-1-p h e n yl-5-m e t h y 1 be n z o tlh i az o 1 e (MORGAN and WEB-C1,,H1,Cl2S2 D i c h l o r o dim e t h y 1 t h i a n t h r e n (RAY) 1963. C14H,,N,C1 5-Ch 1 o ro-J-p 11 e n y 1-6-111 e t h y 1 b en zi min a z o l e (MORGAN and C,,H,,ON .P h e n y 1 gl y ox a l p h en y l h pd r s z o n e preparation tautomerism and CI4Hl20,N4 Ben za 1 d e h y d e d i n i t r o t o 1 y 1 h y draz o n e s (BRADY and BOWMAN), C14H,,0,N3 6-N i t r o-m-x y 1 en e-4-a z o r e so r c i n o 1 ( PEARMAN) 717. ClpH140,N2 D i a m i d e of aa’-d i cya n o-B-b e n z y 1 g l u t a r i c a c i d (KON and C,,H,,O,N 5- and 6-37 i t r o-9-a c e t y l t e t r a h y d r o c a r b az o 1 e s (PERKIN and C,,HI,06N2 p - N i t r o b e n z o y l derivative of B-hydroxy-B-3:4-m e t h y l e n e -C14H14ClBi D i - p - t o l y l c h l o r o b i s m u t h i n e (CHALLENGER and ALLPRESS) 917. C,,H,,ON C14H,,03N Ben z o y 1 a-m e t h y 1 am i n o-p-g 1 y oxali n e-4-pr o-C,,HloON 6-A c e t y 1 amino t e t r a h y d r o car b az 01 e (PERKIN and PLANT) 1833.C14H160,N I n d ole-2-car bo x y-a-(car b e t hox y) e t h y lam i d e ( RERMACK PER-C1,H,,04C1 E t h y 1 m-c hl o r o b enz y 1 ma1 on a t e ( KENNER and WITHAM) 1460. Cl,Hl,OIlNz (Scow and GOHEN) 671. C1,H1,O,N S emi c a r b a z o n e of ac-I -kc to-3-me t h y 1 t e t r ah y d r o n a p h t h y 1-3-acet1 c a c i d (KON and STEVENSON) 91. Cl,Hl,N,I P h e n y !b e nz y 1 in e t h p l a zon i 11 m iodide additive compound of thiocarbamide and (SINGH and LAL) 211. C14H17N4C12 33’-D iam i n o-8-m e t h y l p h e naz i n e me t h o c h 1 o r i d e (COHEN and C14H190N3 cycZoH e x a n o ne-pa c e t y 1 am i n o p hen y 1 h y d r a zo n e (PEEKIN and C,,H,,O,N 6-Ac e t y lam ino-nz-4-x yl yl n-pro p y 1 k e t o n e (MORGAN and C14H210,N 2-Nitro-l:4-di-n-butylbenzene (MORGAN arid HICKINBOTTOM), Cl,H,,O,N S e ni ic a r baz o n e 1-k e t o-3-m e t h y 1 oc t ah y d r on ap h t h yl-3-C14Hs,0,N E t h y 1 o-cyanom e t h s n e t r i a c e t a t e (INGOLD) 340 352.haloids on (MCKESZIE and BOYLE) 1131. STER) 1074. CHALLENOR) ’1543. solubility of (SIDGWICK and EWBANK) 487. 899. STEVENSON) 93. PLANT) 1832. d i o x y phen y l e t h y l it m i n e (RIASON) 1080. 9-A ce t y 1 t e t r a h y d r o c a r b a z ole (PEBKIN and PLANT) 1831. derivative of p i o n i c acid (+$H,O) (FARGHER and PYMAN) 738. KIN and ROl3INSOK) 1628. 4-p-A c e t ox y b enz y l h y d a n t o i n OO-d i m e t h y 1 e t h e r CRABTREE) 2068. PLANT) 1S33. HICKINBOTTOM) 1890. 1892. acetic a c i d (KON and STEVENSON) 93.of 14 IV ClpH,@&Clz Chloride of y-6:6’-di n i t r o d i ph eni c a c i d ( KENNER and C14H,0,NB~2 D i b ro mo-9-n i t rop h e n a n t h r e n e (HENSTOCK) 58. C~~H,ONBP D i b r om o p h en a n t 11 r o n e o x i me ( HENSTOCK) 58. C~4H1004NCl Benzoyl derivative of 2-chloro-5-nitro-pcresol (DAVIES) 867. STUBBINGS) 599. 21’7 FORMULA INDEX. 14 IV-15 III C,4H,,010N,Cd Cadmium d i n i t r o t o l y l o x i d e s (D. and A E. GODDARD), 2048. C14H1001~NlMg Magnesium d i n i t r o t o l y l o x i d e s (D. and A. E. GODDARD), 2048. C~4HloOloN4Sr S t r o n t i u m d i n i t r o t o l y l o x i d e s (D. and A. E. GODDARD), 2047. Cl,H,,Ol0N,Zn C1,HlONClS 4’-Chloro-l-p h e n y 1-5-m e t h y 1 be n z o t h i az o 1 e (MORGAN and ClrH,,ON,S l-P hen yld-me t h yf ben z o t h i a z ole-4’-diaz oni urn h y d roxide, Cl,H,,03N,S2 l-P henyl-5-m e t h y 1 ben z o t h i a z ole-4’-d i a zo s u l p ho n i c acid, C,,H,,O,N,S N-S u l p h i d o b i s b e n za m i d e (NAIK) 1168.Cl,H,,O,N,S, C,,H,,O,N,Ba Barium n i t r o t o l y l o x i d e s (D. and A. E. GODDARD) 2046. ClaHlpO,NaCa Calcium n i t r o t o l y l o x i d e s (D. and A. E. GODDARD) 2046. ClpH,,O,N,Mg Magnesium n i t r o t o l y l o x i d e s (D. and A. E. GODDARD) 2047. Cl4HlaO8N2S~ S t r o n t i u m n i t r o t o l y l o x i d e s (D. and A. E. GODDARD) 2046. C,,H,,O,NBP E t h y l e Y t e r of a-br o m o p r o p i o n y 1-Z-t y r osi n e ( SHIMOMURA Z i n c d i n i t r o t o l y l o x i d e s (D. and A. E. GODDARD) 2048. WEBSTER) 1074.salts of (MORGAN and WEBSTER) 1073 1076. sodium salts (MORGAN and WEBSTER) 1075. D i s u l p h i d obi s-s a l i c y l am i d e ( NAIK) 1169. and COHEN) 1823. Cu GXWUP. Cl6HlOO4 1:6-D i h y d r oxy-2-m e t h y l a n t h r a q u i n o n e 1339. CI6Hl2O2 9-Acetoxyfluorene preparation of (HENSTOCK) 1463. C15H1,OS l-H y d rox y-3-m e t h y 1 x a n t h o n e m e t h y 1 e t h e r ( PERKIN) 1292. C16H1406 Catec hin constitution of (NIERENSTEIN) 164. (QIMORSEN and RAU), 2:4:6:3’:4‘-Pe n t a h y droxy-3-p h e n y 1 c h r o man (NIERENSTEIN) 169. 15 I11 e h 1 or om e t h yl-6-BBB-t rich1 oro-a-h y d r o xye t h y 1-1 :3-ben z d i o x i n e-5-carboxylic acid (ALIMCHANDANI and MELDRUM) 208. 7:s-d im e t h o xy-2:4-bis t ri c h l o r om e t h y 1-6-B-t r i c h l o r o-a-h y d r ox y e t hyl-l:3-b e n z d i o x ine-5-ca r box y l i c a c i d (ALIM-CHANDANI and NELDRUY) 207.C1,H,,N,S (MORGAN and WEBSTER) 1076. Cl,H,,0,C13 3:4:5-Tr i a ce t ox y-2-t r i c h 1 or o m e t h y l p h t ha1 i d e (ALIMCHAND-ANT and MELDRUM) 206. Cl,H,,0,N3 3:5-D i m e t h y 1 is0 o x az 01 e-4-a z o-B-na p h t h 01 (MORGAN and BUE-GESS) 702. C15Hl,0,N1 4-Ni t ro-2-car be t hoxyszo benzene ( EENNER and WITHAM) 1056. Cl5H,,O,N 6-Ni t ro-m-x y 1 en e-4-azo s a l i c y l i c a c i d ( PEARMAN) 718. C15H13N4Br 5 - 8 ni i n o-4-(2’-am i n o-5’-b r om o p h en y 1)-2-p h e n y 1 g l y ox a 1 i n e, Cl5HI40N4 S:5-D i m e t h y 1 isoox az o 1 e-4-a zo-8-11 a p h t 11 y l a m i n e (MORGAN and C,,H,,ON B-A m i no-B-p h en y 1 p r o p iop h e n o n e (MCKENXIE and BARROW) 69.C15H1603NS p-N i t r ob en z a1 do x im e-LV-p-e t h y lamin op h en y l ether (BAKROW C,,H1603N p-N i t rob en ztt 1 d o x ime-N-p-di m e t h y l a m i no p h e n J 1 ether CI5H4OSCllB L a c t o ne of 7:8-BBB-tric h l o r o e t h y 1 i den edioxy-2:4-bis t r i-C1,H,OaC1 L ac t one of 4'-C y ano-l-p h en yl-5-m e t h y l b en z o t h i azo 1 e and its salts (FARGHER) 160. BURGESS) 703. and GRIFFITHS) 215. (BARROW and GBIFFITFZS) ‘214. 217 16 111-16 I1 FORMULA INDEX. C15H150aN 8-0 a r bet b ox y-a-m e t h y 1 v i n y 1 i n d o 1 e-2-ca r box y 1 a t e ( KER-MACK PERRIN and ROBINSON) 1629. C,,H,,O,N N i t r o c a r b e t h o x yh y d r a z o be n z e ne s ( KENNER and WITHAM), 1056. CljHloONz &Am i n o-p-p h e n y l p r o p i o n a n i 1 i d e ( MCKENZIE and BARROW) 71.C,,H,,O,N and its salts C,,H,,O,N 3:5-D icyano-2:6-d i k e t o-4-cycloh e x e n y 1 m e t hyl-4-m e t h y 1 pi-C,,Hi,0,N3 A n t i p y r y l a m i n o d i a c e t i c acid and its salts additive com-C,,H,,ON (PERKIN and Cl,H,,N4Clz 3:7-Diami no-2:8-dim e t h y l p he n a z i n e m e t hoch l o r i d e (COHEN 4-D i m e t h y l am i n o-2-h y d r o x y b e n z h y d r 01, ( ~ R I S H N A and POPE) 287. p e r i d i n e (KON and STEVENSON) 92. pounds of with neutral salts (FARGHER and KING) 292. PLANT) 1835. 6-A c e t y l am i no-9-m e t h y 1 t e t r a h y d ro c a r b az 01 e and CRABTREE) 2067. C,,H,,ON A n i l i d e of l a c t o n i c a c i d Cl0lTl,O4 (BIRCH GOUGH and KoN), 1327. C15H,,03N An i l i c acid from qclo-h ex a n e-l-a c e t i c-l-c a r bo x y l i c a c i d C,,H,,O,N S emic a r ba zo n e of ac-l-k e t o-3-e t h y 1 t e t r a h y d r o n a p h t h y 1-3-CI5H,,O3Na I n do le-%car b ox y a c e t a 1 y 1 amid e ( KERMACR PERKIN aiid C,,H,,O,N Eserine degradation of (STEDMAN) 891.C,,H,,O,Ga Gallium a c e t y l a c e t o n e (MORGAN and DREW) 1061. ClsH21061n I n d i u m a c e t y l a c e t o n e (MORGAN and DREW) 1.062. C,,H,,O,N (NORRIS and THORPE) 1207. a c e t i c acid (KON and STEVENSON) 92. ROBINSON) 1626, E t h y 1 o- and w’-c y a n o-w-m e t h y l m e t h a n e t r i a c e t a t e s ( INGOLD aiid PERREN) 1600 1868. 15 IV Cl,He02NzBr D i br o mo m a10 n-2:4 6-tr i b r o m o a n ili d e (BACXES WEST and C1,H,0,N2Br D i b r om om a1 o n-2:4-d i b r o rn oa n i l i d e (BACKES WEST and Cl,H,Ol,NsS T e t r a n i t r o d i t h i o m e s o x a n i l i d e (NAIK) 383.C15H1002N2Br4 Di bromomalon-p-broinoani l i d e (BACKES WEST and C15Hl10zN2Br Bromomalon-p-brom oan i l i cle (BACKES M 7 ~ s ~ ~ and C,,H,,O,N,Br D i b r o m o ma 1 o n a n i 1 i d e ( BACKES WEST and WE-IImLEY) 375. C,,H,,O,N,S, Cl,H,40NCl 8-m-Chlorophenylpropiona n i l i d e (KENNER and WITHAM), 1460. C1,H,,O,NBr 4-d i m e t 11 y 1 am i n o-2-h y d ro x y-be n z h y d r o 1 ( KRISHNA and POPE) 287. WHITELEY) 375. WIIITELEY) 374. WHITELEY) 374. WHITELEY) 374. D i t h i o ni e s o x a n i 1 i d e (NAIK) 382. D i b rom o-de r i v a t i ve of C, Group. ClaHl,O2 o-Dimethylanthraquinones (FATRBOURNR) 1573. C1,H1,05 acid and its silver salt (SIMOKSEN and RAU) 1346.CleHloAs 431. C,,H,,O, C,,H,,O, 4'-H y dr oxy-2-m e t h o xy-3-m e t h y 1 be n zop h eno n e-6-car b o x y l i c P h e n yl-y-p h e n y 1 prop y 1 me t h y 1 a r s i n e (BURROWS and TURNER), E t h y 1 ?L-b u t a n e-aay6-t e t r a c a r b ox y l a t e (INGOLD) 348. E t h y l carboxyrnethanetriacetate (INGOLD and POWELL) 1873. P a l m i t i c acid sodium salt adsorption by (LAING) 1669. 217 FORMULA INDEX. 16 111 16 I11 C16H,05Nn 9:10-Dinitro-2-ethoxyphenan tlireue (HENSTOCK) 61. ClaHl103N3 Cl,Hl,0N2 C1&12O& C16H,,0eN, C16Hl,0Br C16E1303Na C,,H,,O,N, l - B e n z oyl-4(or 5)-11 i t r op h e 11 y 1 g l y o x a1 i 11 e s (GRANT and PYhlAN), 1-B enzoyl-li(or 5)-p h en y l g l y oxal ine (GRANT and PYMAX) 1899.Diac e t y 1 t h i a n t h r e n (RAY) 1965. M e t h y l y-6:6’-dinitrodiyheiiate (AEvsER and STUBBIKGS) 599. 10-R romo-2-e t h ox y p he n RII t h r e n e (HEXSTOCK) 60. 5 u b s t a 11 c e from benzenediazonium chloride and 4 -p-hydroxybenzyl-Car b e t h o x yam i 11 o p h en an t h r i d o n e ( KENHER and STUBBIKGS), 1899. hydantoin ( S c o T r and COHEN) 671. 601. Phenylopiazones (FARGHER and L’ERIIIN) 1743. Anilino-m-opianic a c i d (FARGHER and PERKIN) 1739. Y II b s t a Iie c from anilino-m-opianic acid and hydrochloric acid (FARGHER and PERKIN) 1740. C,,H150pN3 4-n it ro-2-ca r b e t h ox y p he n y 111 y d r a zo n e (KESXEE and WITHAM) 1055. C16H1603Nn n-Bu t y r o p hen o n e-3-3 z o r es o r c i no 1 ( MORGAN aud HICKIN-UOTIUM) 1884.Cl6Hl6O5N4 3-N i t ro-4-h y d rox y pli en y 1 n-p r o p y 1 k e t o n e p-ni t r o p h e n y 1-hydrazone (MORGAN and H1CKINBorTObl) 1888. C1,Hl,0,N3 Y h e 11 y 1 m-p r o p y 1 k e t o n e p-ni t r o p h e n y 1 h y d raz o n e (MORGAN and HICKINBOTTOM) 1882. ClaH1,O,Ns 3.H y drox y pli en y1 n-prop y 1 k e t o n e p - n i t r o p he n yl-C,,H,,N,Cl 4-C h 1 or op h e n y 1 n-pr o p y l k e t o n e p h e n y 1 h y d r a zo n e (MoR-Cl,H,,0,N2 5-H y d r ox y-4-me t hox y-o-t 01 y 1 m e t h y 1 k e t on e ph en y 1 h ydr-ClsH,,O,S BB’-D i p h e no x y d i e t h y 1 d i s u l p h i d e (BENNETT) 425. ~16H,,0sN o- and p-Nitrophenyliminocamphor (FORSTER and SAVILLE), C16H,aO& 3 :5:3’:5‘-T e t r a k e t o-4:4’-b i s d i t h i 0-1 :1 :l’:l’-t e t r a m e t h y 1 d ieyclo-Cl,HloON A n i l i d e of mjclop e n t a n espirocyclo h e x a u e-3:5-d io n e (NORRIS and C16Hl,04N3 o- and p-N i t r o p 11 e n y 1 n i t r o s oa m i n oc am p h or (FORSTER and C,,Hls05N3 C,6HlsN,I P h e n y 1 be n z y l a 11 y l a z o n i u m iodide additive coinpound of thiocarbamide arid (SINGII and LAL) 211.Cl,H,,0,N2 N-P h en y 1 camphor i m i d oxi m e P h e n y 1 n i t r 0 s o anii n o-c a nl p h o r (FORSTER and SAVILLE) 792. C16H20N4C1s m e tho-c 11 1 o r i d e (COHEN and CRABTREE) 2058. C,,H,lON l’h e 11 y 1 a m i n o c am p h o r hydrochloride of ( FoRsr ER and SAVILLE), 791. Cl6HZlN2I P 1.1 en y 1 be n z y 1 p r o p y 1 azo n i u in iodide additive compound of thiocnrbamide and (SINGH and LAL) 211. Cl,H2,0Ns p-Amino phenylaminocamphor and its dihydrochloride (FORSTER and SAVILLE) 794.C1,H,,0sN2 l-M e t h y 1 i n d 01 e-2-c a r b o x yac e t a 1 y 1 am i d e ( UEKMACK PEKKIN, arid ROBINSON) 1637. S c a t ole-2-car box yac e t a1 y la ni i d e (KEKMACK PERKIN and ROBINSON) 1635. Cl6Hl5O4N Ben z a I d e h y de hydrazone (MORGAN and HICKINBOTTOM) 1885. GAN and HICKINBOTTOM) 1886. azolie (FAILGIIEL~ arid PERKIN) 1733. 794. h e x y I 2:2’-d i s u l p h i d e (NAIK) 1240. THOKPE) 1207. SATILLE) 793. Dinitrophenylamin ocamphor (FORSTER and SAVILLE) 792. and 3-Am i n o-7-dim e t h y laini n o-2-m e t h y lp hen a z i n e 217 16 111-17 I11 FORMULA INDEX. C1,H2,04N 6-M e t h ox y i n d o 1 e-2-ca r b o x y ac e t a 1 y 1 a m i d e (KERMACK PER-KIK and ROBINSON) 1633.16 IV Ci,H,O,N,S N-Sulphidodiph thaliniide (NAIK) 1170. C,,H,,O,N,S 5-D i s u l p h i d o-1:3-d i p h en y 1 b a r bi t u r i c a c i d (NAIK) 385. C,,H,,ONBr D i b r om o-9-a ce t y l a rn i n op h en a n t h r e n e (HENSTOCK) 59. Cl,H,,0,N4Br 4-p-B r om obeii z e 11 eazo-2-phe nylglyoxaline-5-car b ox y l i c C,,H,,O,N,Br 5-B r om o- 1:3-d i p 11 en y 1 barb i t u r i c acid (BACKES WEST and C,,H,,ON,S 2-Ac e t yl-3-oxy(l)th ion a p h t hen p h en y 1 h y cir az one (SMILES C,,H,40,N,S Diac e t y lam i n o t h i a n t h ren (RAY) 1964. C,,H,,O,N,Cl 3:4-D i c h lorop hen y 1 qz-pr opy 1 k e t o n e p - n i t r o p h e n yl-hydrazone (MORGAN and HICKINBOTTOM) 1889. C,,H,,O,N,Cl 4-C hloro-3-n i t r o p h e n y l n-propyl k e t o n e p-ni t r o p h e nyl-hydraz one (MORCAN and HICRINI~O~~TOM) 1888.CIBH1602NSC1 4-C h 1 o r o-3-n i t r o p hen y l w p r o p y 1 k e t o n e p h e n y l h y dr-azone (Monaa~ and HICKIXBorwhf) 1888. C lilor op h en y l n-pr o p y l k e t o n e p-ni t r op h en y l h y d razone s (MORGAN arid HICKINBOTTOM) 1885. acid and its sodium salt (FARGHER) 159. WIIITELEY) 375. and MCCLELLAND) 1814. CI7 Group. C,,H,O, (MILLS and NODDER) 2099. C17Hl,0, NODDER) 2102. C1,H1404 1347. Phenolcitraconein and its potsssium salt (KRISHNA and POPE) 289. Cl,H,,As Phen yl-a-n a p h t h y lni e t h y l a r s i n e (BURROWS and TURNER) 432. C,,H1,O Eugenol benzoates melting points of (Mcl<r~) 777. Cl,H1605 2:4’-D i me thoxy-3-m e t h ylbe n zophen one-6-car b oxylic acid and C,,H,,Br Hvdrocarhon froin petroleum extract of the bromination of phen-Cl,Hl,O C17H2,0 C,,H,,O E t h y l cyclope n t a n e-1:2:2:3-te t rac nr b ox y l a t e (PERKIN and 17 111 be n z o p h en o n e-2:4:2‘:4’-te t r a c ar box yl i c 7:8-di ace t o xy-2:4-bis t r i chlor om e thyl-6-B-t ri-a c i d (ALIM-Ben z o p h en o ne-2:4:2’:4’-t e t r a c a r bo x y l i c k e t o d i l a c t on e B e nz h y drol-2:4:2’:4’4 e t racar bo x y l i c a c i d lac t one (MILLS and 1:6-D i m e t h o x y-2-m e t 11 y 1 a n t 11 ra q u i n o n e (SIMONSEN and RAU), a c i d its silver salt (SIBIONSEN and RAU) 1347.antlirene (HENSTOCK) 60. Di-rlz-xylyl ketone preparation of (MILLS and NODDER) 2099. B e n zyli d e 11 e-cll-pipe r i tone (READ and SMITH) 784. R o u r ~ s o ~ ) 1397.Cl,H6qSClO A c i d CI7H,O8C1 Lac t one chloride of a c i d k e t o d i l s c t o n e (MJLLS and NODDER) 2100. ch loro-a-11 y d r o x y e t h yl-l:3-benzd i o x ine-5-carbox ylic CHANDANI and MELDRUM) 207. of C17Hlo0,Br4 Tetrabromophenolcitraconein (KBISHNA and POPE) 290. C,,H,,N,Cl (MORGAN and C,,H,,ON A n i l i d e of cyclohexanespirocycZohexane-3:5-dione-3:5-dione (KOREIS and C1,H,,O2N D i h y dro x y n a p h t h y l i den ean i 1 i n e s (MORGAN and VINING) 179. C,,H,sO,N B-Ph t h a l i n i i n o-8-p h e n y l p r opioni c acid (MCKENZIE and 10-Ch l o ro-9-m e t h y I-a&n ap h t h a p h e naz i n e CHALLENOR) 1540. THORPE) 1206. BARROW) 73. 218 FORMULA INDEX. 17 111-17 IV C,,Bl,OsNz 2-Ca r b ox y i n do1 e-S-ac e t a n ili d e (KERYACK PERKIS and C17H150As P hen y 1-a-n a p h t h y lm e t h y 1 a r s i ne oxide( BuRROw~ and TURNER), C17Hl,0aN Anilin 0-4:5-dime t h ox y p h t h a l o n i c acid aniline salt (FARGHER Cl,Hl,O,N 1-T o In en e-p-su 1 p h on y In a p h t h y l e n e d i am i n e s u l p h o n i c Cz7H1,O2N 3-Benzoylaminophenyl ?t-propyl ketone (MORGAN and HICKIN-C1,H170*As h y d r ox i d e, bromocamphorsulphonate of (BURROWS and TURNER) 432.Cl,Hl,04N M e t h y l anilino-?n-opianate (FARGHER and PERKTN) 1741. p-To1 u i d i n o-m-opianic a ci d (FARGHER and PERKIN) 1739. Cl,Hl,02N D ian ilinoa c e t y 1 acetone (MORGAN and DREW) 622. Malondibenzylamide (BACKES WEST and J T 7 € i I ~ ~ ~ ~ y ) 370. C,,Hl,OpNa a’-Di h y dr ox y gl u t a r d ia n il i d e s (IXGOLD) 323. Opianic a c i d phanylmethylhydrazones (FARGHER and PERKIN) 1743.C17H1,0N B enz o y 1-.n-bu t y l a n i l i n e (MILLS HARRIS and LAMBOURNE) 1298. C1,H?,O,N 4-D im e t h y 1 ami n 0-24 c e t ox y b en z h y d r 01 ( KBIYHNA and POPE), 287. CZ7HI,0,Ns p-N i t r o b e n z a ldo xime-N-p-di e t h y l a m i n ophe n y 1 e t h e r (BAR-ROW and GRIFFITHS) 215. C,,Hl,N2C1 6(7)-C h l or o-T(G)-m e t h ylc a m p h an o quin o x a l i n e ( MORGAK and CHALLENOR) 1540. ROBINSON) 1625. 432. and PERKIN) 1738. acids and their sodium salts (MORGAN and GRIST) 608. BOTTOM) 1884. H y dro x y ph e n y l-a-n a p h t h ylni e t h y l a r s on ium c17H2,0,N D i-p-ni t r o p hen y l h y d r azi n o ac e t y l a c e t o n e (MORGAN and DREW) 621. Cl,H,,ON A n i l i n o m e t h y 1 en e-e pic amp hor (PERKIN and TITLEY) 1100.Cl,HaaIAs P he nyl-7-p h en y 1 p r o p y 1 met h y 1 a rs ine me t h i o d i de (BURROWS C17Ha405Na 1:3-D ime th y l i n d ole-2-carb ox yace t a l y 1 amid e (KERMACK PER-CZ,HzB08N E t h y l a-c yan o-.n-bu tane-aSy8-t e t ra c ar b ox y 1 a t e (INGOLD) 348. Benzy 1 idene-dl-piperi t o n eoxime (READ and SMITH) 788. and TURNER) 431. KIN and ROBINSON) 1637. 17 IV C,HI,O,NCl 8-P h t h a l i min o-B-p h e n y 1 p r op ion y 1 c h 1 o r i d e (MCKENZIE and Cl,H,20,,WsS1 Te t r a n i t r odi t h i o m e s o x o t o l u i d i d es ( NAIK) 1235. C17Hl,02N2B~ D i h y d r o x yn a p h t h a1 de h y d e p h e n y 1 hydra zo n es ( MOEGAX G,H,,O,N,BP D i br omo m a 1 on b r om o t o l u i d i de s (BBCKES WEST and C,,H1,O,N,S ay-D is u l ph i d o ace t o n e d i c ar box y d ia n i l i d e (NAIK) 1240.C,,H,,O2NaB~ Bromornalon-4-br omo-o-t o lu id id e (BACKES WEST and WHITELEY) 377. C1,Hl6O2NaB~ Di br om om a1 o ndib e n z y la mi d e (EACKES WEST and WHITE-LEY) 371. BARROW) 73. and VINING) 178. WEIITELEY) 376. Dibromomalon-p-toluidi de (BACKES WEST and WHITELEY) 376. BIalon bromotoluidides (BACKES WEST and WHITELEY) 376. C,,H,,O,N,S T olu en e-psul p honpl-l:4-n ap h t h y lenediam i n e (MORGAN and C,H,O,N,S D i t hiomca ox o d i b en z y l a mid e (NAIK) 384. GRIST} 604. Di t hiomesoxotoluidides (NAIK) 1235. 218 17 IV-I8 I11 FORMULA INDEX. C1,HleO,NCl P he n y l c h l or o a c e t y 1-Z- t yr o s i n e (SHIMOMURA and OHE EN) 1824, C,,H,,O,N,Cl t o l y l e n e d i a m i n e (MOPGAN and JONES) 188.C,,H,,O,N,Br 370. C,,Hl,0,N4C1 D iace t y 1 derivative of 4’-n i t r o ben z e n e-6-az 0-642 h l o r0-2:4-B r o m o ni a1 o n d i be n zy lam i d e (BACKES WEST and WHITELEY), B r o 1n omalo n-p-t 01 u i d i d e (BACKES WEST and WHITELEY) 376. Diac e t y l derivative of benzene -5-azo-6-c h l oro-2:4-t 01 y 1 en e. diamine (MORGAN and JONES) 188. CIS Group. C18H1605 Pipe ron y li d en e derivative of 5-h y droxy-4-m e t h ox y-o-t 01 y 1 Cl8HI8O3 Benzyli d ene derivative of 4:5-dime t hox y-o-t 01 y 1 m e t h y l k e t o n e ClsH1,O5 Methyl 2:4’-dim e t h o x y-3-m e t 11 y 1 be n z op h e n on e-6-ca rbox y l a t e C1,H2,0 Be nz o y l o x y me t h y l e n e-e p ic a m p 11 or (PERKIN and TITLEY) 1099. C18HaoOz L i n o l e n i c acid and its salts (COFFEY) 1306 ; oxidation of (COFFEY), 1409.C18H& L i n o l i c acid oxidation of (COFFEY) 1408. ClRHl108NP “ D iace t y 1 hydra zid e )) of y-6:6‘-d i u i t r o d i p h e n i c a c i d ( KENNER C,,H,,ON Cinnam oy 1 am i noq uino 1 i n es ( HAMER) 1437. C18H,,0,N Met h y 1 6-13 h t h a l i m i n o-B-p h e n ylpropio n a t e (MCKENZJE and BARROW) 74. C18H,,06C1 8sB-T r i c h l or 0-4:4’-d i h y d ro x y-aa-d i-m-t o 1 y l e t h a n e-5:5‘-di-c a r b o x y l i c acid and its calcium salt (ALIMCHANDANI aud MELDRUM) 209. C18Hl,0,N2 y-6:6‘-D iac c t y l a m i nodi p h en i c a c i d ( KENNER and STUBBINGS), 600. Cl8HlsO8N2 E t h y 1 y-6:6’-dinitrodiplienate (KENX’ER and STUBBIKGS) 599. C18H1608N D i n i t r o-2:3:6:7-t e tr,a m e t h o x y a n t h r a qu i none d i-im i d e C18H1706N p-T o l u i d i n o-4:5-d i me t h o x y p h t ha 1 o n i c a ci d p-toluidine salt C18H1700N8 D i a c e t y 1 derivative of 6-n i t r o-nz-x y 1 en e-4-a z or esor c i n 01 (PEAR-ClaHleOpN2 2:3:6:7-T e t r a m e t h 0 x y a n t h r a q II i n one d i-i mi d e (KEFFLER) 1480.C18H1806NI E t h y 1 i d e n e b i s-p-n i t r o p h e 11 y l a c e t am i d e (GUPTA) 302. Cl8H1,O,N o-A zoxy-p-m e t h oxyp hen y 1 a c e t i c acid ( KERMACK PEHKIN and C18HlaN4C1 Te t r am e t h y 1 ene bis-2-chlo r o-4:S-d i a tn i 11 o t o 1 u e n e (MORGAN C1sHl,IAs P hen y l-a-na p h t h y 1 in e t h y l a r si n e me t h iodide (BURROWS and C1,H,,02Na 6:6’-D iac e t y 1 am i n o-2:2’-d i t 01 y 1 (KENNER and HTUBBINGS) 600. Met h y lm alono t o l u i d i d e s ( NAIK) 1238.ClsH,102N m-4-X y 1 y 1-?%-pro py 1 k e t o n e p-n i t r o p 11 e n y 1 h y d r a z on e (JSToa-GAN and HICKINBOTTOM) 1889. C,8H,lN,C1 3 - 8 m i II o-2-m e t h y I-N-in e t h yl t e t r a h y d ro q u i n o l i n op h e n a z i n e methochloride (COHEN and CRABTREE) 2065. Cl,H2,0,N P h e n y 1 ace t y l a in i n o c a m p h o r ( FORSTE it and SAVILLE) 791. Cl,H2,02C1 E-Menthyl dl-phenylchloroacetate (SHIMOMURA and COHEN), 2182 m e t h y l k e t o n e (FARGHER rind PERKIN) 1733. (FARGHER and PERKIN) 1732. (SIMONSEN and RAU) 1346. 18 I11 and STUBBINGS) 600. (KEFFLER) 1481. (FAI~GHER and PERKIK) 1739. MAN) 717. lio BIKSOX) 1631. and CHALLBNOR) 1641. TURNER) 432. 1818 FORMULA INDEX. 18 111-19 I11 C,,H,,O,Br C,,H,,O,N C1HH3002BP6 Hexabromostcaric acid and its salts (COFFEY) 1306.ClsHnO,N T ri(di e t h y 1 am i noni e t h y 1) Z-RI e n t h y 1 dZ-p h R n y 1 b r omoace t a t e (SHIMOMURA and COHEN), E t h y 1 w-c ya n o-w’-c a r b o x y-w”-m e t h y 1 methane t r i a c e t a t e (Is-1820. GOLD and PERREN) 1599. gl y c e r y 1 e t h e r ( MCLEOD and EOBINSON) 1473. 18 IV ClsH160sNzSs SS‘-D i-p-n i t r o be n zo y 1 d i e t h y l C,8H,40NCI C,,H2aONC1 d i s u 1 phi d e (BENNETT and Phen y l c h l o roace t o-d-bor n y lam i d e (SHIMONVRA and COHEN), P h en y l c h lo r o ac e t o-l-m e n t h y 1 amid e (SHIMOMURA and COEEN), WHINCOP) 1861. 1823. 1823. CI9 Group. ClsH13N ti-phenylacridine picrates of (BASSETT and SIMMONS) 417. ClsHI4OB A c e t y 1 derivative of 1 :6-d im e t h o x y-2-m e t h y 1 a n t h r a q u i no n e (SIMONSEN and RAU) 1347.ClsHlaOa F l u o r a n derivative of c i t r a c o n i c a n h y d r i d e (KRISHNA and POPE), 291. C,,Hl,O4 P h e n o l c i t r a c o n e i n d i m e t h y l e t h e r (KRISHNA and POPE) 290. ClSHIOOB 4:6:3’:4’-Te t ram e t ho x y-3-pheny lc h rom an-%one (NIEBENSTEIN), 167. C1eH220 2-Hydroxy-4:6:3’:4’-te t rame t h oxy-3-ph e n y lchroman (NIEREN-STEIN) 168. C1sH2e03 Z-B o r n y 1 a-h y d rox y-S-p h e n y l p r o p i o 11 a t es (WREN and WRIGHT), 802. ClsHZsO3 Z-Men t h y 1-d-a t r olac t i n a t e (WREN and WRIGHT) 800. C1sH36021 C,,H,,NBP A n t h r a n y l p y r i d i n i u m bromide ( f HSO) (BARNETT and COOK), 907. ClSHl50N A n t h r a n y l p y r i d i n i u m h y d r o x i d e salts of (BARNETT and COOK), 90;.C,,H160N2 C in n am o y lam i n oq u i n a Id i n es (HAMER) 1437. ClsHl,04N3 Anhydride of 2-carboxyindole-3-acetanilide and acetic acid ( KER-C,,H,,ON 6-Benz o ylam i n o t e t r a h y drocarba z ole (PERKIN and PLANT), Cl,Hl,O,N cycZoPen t a n 0 ne-3:4-d i car bo x y a n i l i d e (INCOLD) 350. ClsH,,O,N 4’-D ime t h y 1 am i n o-2-h ydrox ydis t y r y 1 ketone and its additive ClrHzoOaNa A ce t on c d i c a r b ox y d i t o l u i d ides (NAIK) 1241. C,,H,O,N D i a n i l i c acid from m e t h a n e t r i a c e t i c a c i d (INGOLD) 353. Cl,H,03N H y d pox y l a m i no-derivative of 4‘-di m e t h ylamin o-2-h ydr o xy-d i s t y r y l ketone (HEILBRON and BUCK) 1518. C,9H2204N2 a d - D i h y d r o xyglu tardi-p-t oluid i d es (INGOLD) 323.ClDHza03N3 H yd roxylami n o-derivative of 4‘-dime t h y lam ino-2-h y d r oxy-p-N i t r o be n zaldo x im e-N-p-di-n-pro p y lam i n o p h e n y 1 e t h e r (BARROW and Z-M e n t h y 1-Z-a-h y d ro x y-B-p 11 en y 1 prop i o n a t e (WREN and WRIGHT) 802. 19 111 Hex am e t h y l m e t h y 1 cello bio s i d e (HAWORTH and HIRST) 198. MACK PERKIN and ROBIP~SOX~) 1625. 1833. prodocts (HEILBRON and BUCK) 1600 1515. d i s t y r y l ketoxime (HEILBILON and BUCK) 1518. GKIFFITHS) 215. CleH2,0,Na E t h y l a n t i p y r y l a m i n o d i a c e t a t e (FARGHER and KING) 297. 218 19 111-20 I11 FORMULA INDEX. C,,H,,O,Bp Z-M e n t h y 1 dl-a-brom o-B-p h en y 1 pro pion a t e (SHIMOMURA and COHEN) 1821. 19 IV CloH1,0NBr8 An t h r any1 py r i d i n i um per b r o m i d e (BARNETT and COOK), 907.ClaH1,0N21 Ci n na m o y 1 amino q u i n o l i n e m e t h i o d i d e s (HAMER) 1437. CloHlsOaNsSp a?-D i s u l p h i d o a c e t o n e d i c a r b o xy d it o 1 u i d i d e s (NAIR) 1241. CloHloONPI P h e n y l h y d r a z i n e derivative ( + 3H,O) of s u b s t a n c e C,H,O,t CloHzoOoNCl E t h y 1 e s t e r of p h en y l c h 1 or0 ac e t yl-Z-t yrosine (SHIMOMURA (COLLIE and RELLLY) 1554. and COIIEN) 1824. C, Group. C2,H,,0 D i n a p h t h a-l:7 l‘:7’-diq u i n one (MORGAN and VIXING) 1707. C2,H,,N Amino p h e n a n t h r a p h e n azin es (WATSON and DTJTT) 1215. C2,H,,0 P h e n ol p h t h alein preparation of (WARD) 850. 1 :7:1’:7‘-Te t r a h y d r o x y d i n a p h t h y 1 (MORGAN and VINING) 1712.C20H14No D iam i n op h e n a n t h r a p h e n az i n e s (WATSON and Dum) 1215. C,,H,,N 2:’i’:ll-Triamin op h e n a n t h r a p 11 e ua z i n e and its hydrachloride (WATSON and DUTT) 1217. C2,H1,0 T r i p h e n y l v i n y l alcohol constitution of (MCKENZIE and BOYLE), 1131. CzoHleN4 2:7-Diamino d ih y d r opli e nan t h r a p h e n a z i ne and its hydro-chloride (WATSON and DUTT) 1216. C2,Hl,N 9-P h e nylamino-9:lO-dih y d r o a n t h r a c ene (BARNETT and COOK), 909. C2,HlsOo m-O‘pianic a n h y d r i d e (FARGHER and PERKIN) 1742. C2,H2,0 W-H y d r ox y-3:4:2’:4’:6’-~ e n t am e t ho x y-aa-d i p h e n y 1 p ropan-&on e CzoHarN Baa e from formaldehyde and 4:6-diamino-m-xylene (PEARMAN) 720. C,,H,,O, H e p t a m e t h y l m e t h y l o e l l o b i o s i d e (HAWORTH and HIRST), 199.20 I11 CaoH1,ClpS2 S u b s t an c e from a-chloronaphthalene and sulphur chloride (RAY), 1964. CZoHl2O4N8 D i n aph t h a-l:7:1’:7’-d i q u i n o n e d i o x i me (MORGAN and VINING), 1711. C2,H140sNs 2:7-D i h y d r oxp d i h y d r op h e na n t h r a p henaz i n e (WATSON and DUTT) 1217. C2,H14C1Bi Di-a-naphthylchlorobismuthine (CHALLENGER and ALLPRESS), 918. C20H1602NI 9-N i t r o p h en y lam ino-9:lO-di h y d r a a n t h r a cen e s (BARNETT and C2,H1,02Ns (MORGAN and HICKIN-C2,H1,ON (MORGAN and C20H1D02N, C2,H,,BrAs P h e n y l-a-n a p h t h y lme t h y 1 a 11 y 1 a r s o n i a m bromide (BURROWS C20H210pN 4’-Dime thylamino-2-methoxydistyryl ketone andits additive CPlH2101N4 (KEF-( NIERENSTEIN) 166.COOE) 909. n-B u t y roph en o ne a z o-B-na p h t h o 1 s n-B u t y r op h e non e-3-azo-B-nap h t h y l a m i n e BOTTOM) 1884. HICKINBOTTOM) 1884. 6-Ac e t y 1 ami n o-m-x y l e n e-4-a z o-&n a p h t h o 1 (PEARMAN) 718. and TURNER) 434. compounds (HEILBRON and BUCK) 1509. FLIER) 1482. 2:6-Di me t h oxy-3:7-di e t hox y a n t h r a quinon e d i-i m ide 218 FORMULA INDEX. 20 111-21 I11 C2,Ha40N2 4-Aniino-l-naphthylaminocamphor and its hydrochloride C2,H2,02N2 Quinine hesabromostearate of (COFFEY) 1309. C,,H,,O,N I3 y d r o x y l a m i n o-deiivative of 4’-d im e t h y 1 a mi 11 o-2-m e tli o sy-(FORSTER and SAVILLE) 797. d i s t y r y l lie t o s i m e (HEILBKON and BUCK) 1515. 20 IV C2,H,,OaN2S C2,H,,0N21 C i n n a m oy lam i n o q u i n a l d i n e In e t hio d i d e s (HAMER) 1437.N a p h t h a1 ene-a- and -B-s u 1 p ho nyl-1:4-n a pli t h y 1 en e d i a m i n e (MORGAN and GRIST) 605. Csl Group. C2,H,,0 R cs o r c i no1 c oumar ein (KRISHNA) 1424. C,,H,,O E t 6 yl b en z op h en on e-2:4:2’:4‘-t e t rac a r b oxyl a t e 1; e t o d i l a c t one (MILLS and NODDER) 2101. C2,Hl,O D i a c e t y l derivative of p h e n o l c i t r a c o n e i n (KBISHNA and POPE), 290. CzlHloN (EARNErT and COOS) 912. 9-PI1 en y 1 m e t h y l am i n o-9:lO-d i h y d r oan t 11 race n e 9-To lylamino-9:lO-d i h y d r o a n t h r a c e n e s ( BARNETT and COOIi) 910. C,,H,,O Phenolcoumarein and its salts (KRISHNA) 1430. C2,HalBi Tri-az-tolylbis m u t h i n e (CHALLENGER and ALLPRESS) 920.C21H2204 P h e n o l c i t r a c o n e i n d i e t h y l e t h e r (KRISRNA and POPE) 291. C21H2804 Met h y 1 en e b i scyclo p e n tan e spiroayclo h ex a n e-3 :5-d i o n e (NORRIS and THOKPE) 1208. 21 111 CzlHlzOsBr4 Te t r a bro m o ph enol c oumar e i n ( KRISHNA) 1424. C2;H,,0,Br4 T e t r a b ro mor e s orci n o l coumar e i n ( KRISHNA) 1425. C2,H,N2Cl 5-Ch 1 o ro-2:3-d ip hen y 1-6-me t h y lq u i n osa 1 i n e (MOBGAN and 6(7)-C h l o r o-2:3-dip henyl-7( 6)-me th y 1 quinox a1 i n e (MORGAN and CRAL-GLOVER) 1706. LENOR) 1539. C,,H,,O,Br Ph en oldi br omoc oumarein (KRISHNA) 1421. C2,H,,02N 9 - 0 4 a r b oxyph en y l a ni ino-9:lO-d i h y d r o a n t h race ne ( BARNETT CzlH1,O2N 6-D im e t hylamino-3-h y d r o x y-9-ph e n y 1 x a n t h e n ( BRISHNA and C2,Hl,N21 1 :l’-D i me t h ylisoc yan i n e iodide (HAMER) 1439.CZ1HW1O4C1 E t h y l di-n-c h l o r o benz ylmalona t e ( KENSER and WITHAM), 1460. C2,H,,N,I Am i n 0-1 1’-dimet h y lisoc y a n ine i o d i d e s ( HAMER) 1443. C,,H2,0,N Ace t y 1 derivative of 4 ’ 4 i m e t h y l a in i n o-2-h y d r o x y d i s t y ry 1 k e t o n e (HEILBRON and BUCK) 1509. C2,H2,02N2 S t r y c h n i n e hexabromostearate of (COFFEY) 1309. Cz1H2,0N B-N a p h t h ylamino m e t 11 yl e ne-ep ic am p ho r (PERKIN and TIT-LEY) 1100. C2,H2,0N2 pp’-Te t ram e t h yldiam ino d i s t y r y 1 k e t o n e (HEILBRON and Cz1H2102N4 S e mi c a r baz o n e of 4’-dim e t h y lam ino-2-m e t h o x y d i s t y r y 1 CalH2,0N 2-Ben z o y lamino-l:4-di-n-bn t y 1 benzene ( MOI~GAPJ and HICEIN-C2,H2,O8N4 S e m icarbazi d e derivative of 4’-di me t h y lam i n o-2-h y d r oxy-d i s t y r y l ketone aemicarbazone (HEILBRON and BUCK) 1519.and Coori) 910. POPE) 288. BUCK) 1514. k e t o n e ( UEILBRON and BUCK) 1619. BOTTOM) 1893. CXIX. 2185 4 22 11-23 IV FORMULA INDEX. C22 Group. C2,Hl0O4 C2,HwSi2 C,,H160N, C,,H1,O,N ClaHzlON C2,H,,03N 4-D iin e t h y l a m i n o-2-b e nz o y lox y b en z h y d r 01 (ERIsHNA and C,,H,,O,N B n tyro-2:4-dime t h y 1 11 henone-5-azo-8-naph t h 01 (RIoaam and C,,H,,O& 1:l’-D icyclo h ex a n espi~o-3:5:3’:5’-t e t ra k e t 0-4:4’-b i s d i t h i o dicycZo-C2&2&& p-N i t r o b e nze n c az op h en y l a m i n 0 c a m p h 0 r (FORSTER and SA-C,,H,,O,N Mit raversine and its hydrochloride (FIELD) 891.C22H310,N Rlitragynine and its salts (FIELD) 888. C,2H1,03NaCla NER and WITHAM) 1459. C,2H240,N2S, 719. C,,H2,0,N3S p - S u l p h o benz e n eaz op h e n y 1 amino c am p h o r ( FORSTER SAVILLE) 796. C22H260,N4Sz 3% e t h y 1 m a1 on o m on o-o-t o l u id i d e d i s u l p h i d e (NAIR) 1238. 1:2-Ph t 11 a1 o y l a n t 11 r a q LI i n o n e ( FAIRBOU~LNE) 15SO. dl-D i p hen y l d i e t h y 1 d i p rop y l s i l i c o e t h a n e (KIPPIXC;) 648. 22 I11 1-11 e t h o sy-2-m e t h y 1 p h e na n t h r a p h e n a z i ne B-B e n z oy l a m i n o-Is-p h en y 1 p r o p i op h en0 n e (SiMomm and (MOKENZIE and KAU) 1343. BARROW) 7 3 . (KRISIINA and POPE) 288. 6-D i me t h y lam i n 0-3-h y d r 0 xy-9-p h e n yl-2-m e t h y l x a n t hen I’OPE) 288.HIcmNBoTroJf) 1890. liexylene-2:2‘:6:6’-bisdis u l p h i d e (NAIK) 1240. VILLE) 796. 22 IV ’ E t h y 1 aa-bi s-3-c h 1 o ro-2-c ya n ob e nz y 1 ace t o a c e t a t e (KEN-D i-p-t o lue n e s u l p h o n yl-4:6-d iam i n o-m-x y 1 en e ( PEARMAS), and CZ3 Group. C2,H3,04 Met 11 y 1 en e bi scyclo h ex a n espirocyclo h e xan e-3:5-di o n e (NORRIS and TIIOEPE) 1206. 23 I11 Cz3H1206S2 Met h ylene bia-(1)thionap h t h a-4-oxycou mar i n (SMILES and C2,H1,03N 8-P h t ha l i m i n o-Is-p he n y l p r o p i o p h en o ne (MCKENZIE and BAE-C2,H1,08N2 8-Ph t halim i n o-B-p he n y l p r opionan i l i d e (MCKENZIE and BAR-MCCLELLAND) 18 16. ROW) 75. ROW) 74. C2,HI,0,N C,,H2,O,Nz C2,H2,0,N2 Ben z o y l derivative of p h e n y 1 c a m p h o r im i d e ( FORSTER and C23H2602N2 (FORSTER and SA-B-Ben z o y 1-a-p h en y l e t h y 1 p h t h a l a m i c E en z y 1 i d en e b i s p h e n y 1 ace t a m i d e (GUPTA) 300.a c i d (MCKESZIE and BARROW) 75. SAVILLE) 792. VILLE) 795. (NAIK) 1236. p-Be n zo ylam i n 0 ph en y l a M i n 0 c an1 p h or 23 IV C,,Hl,O,,N,S 13 ex an i t r o-derivative of oxy t h i omes o xo-a-n ap 11 t h y 1 n m i d e C,,H,,0,,N6S2 T e t r an i t r o d i t h i o me a o xo n a p h t h y l a m i d e s (NAIK) 1236. C28Hl,02N2S2 D i t h i om e s oxon a p h t h y 1 am i d e s (NAIK) 1236. C23HnON,I 1441. Ace t y lam i n o-1:l’-dim e t h y 1 isoc y a n ine i o d i d e s (I~AMER), 218 FORMULA INDEX. 24 11-26 I1 C, Group. C2,H,,Na Dicarbazyls isomeric (PERKIN and TUCKER) 221.C,,H,,N 9-B-Na p h t h y l a ni ino-9:lO-di 11 y d r o a n t h r a c e n e C2PH2104 P h en o 1 coumar e i n t r i m e t h y l e t h e r ( KRISHXA) 1423. C24Ha8Si dl-D i b en z y 1 d i e t h y 1 d i pr o p yI si 1 i c o e t h a n e ( KIPPING) 649. 24 I11 C,,H,,N,Br 9:10-D i h y d r oan t h r a q u i n y l d i p y r i d i n i u m d i b romid e (BAR-C2,H,,N2Br 9:lO-Di h y d r o a n t h r a q u i n y l d i p y r i d i n i u m p e r bromi de ( BAR-C,,H2202N2 9:lO-D illy d r o a n t h r a q u i n y 1 d i p y r i d i n i u m di h y d r o x i d e salts C,,H,2BrAs b r o m i d e C,,H,IAs Phe n y l-or-n apli t h y 1 b c n z y 1 m-e t h y 1 a rs o n i u m i o d i d e (UURRCJWS C,,H,,OAs PI1 en y 1-a-n a p h t 11 y 1 I) c n z y 1 m e t h y 1 a r s o n i 11 in h y d r ox i d c salts C,,H,,O,N P 11 en y 1 e t 11 y 1 id e n e b i s p h e n y 1 ace t am i d e (GUITA) 302.C:21H3,03N2 An i s y 1 i d e n e b i s 1) 11 e n y 1 ace t a m i d e (GuP~A) 301. C24H1BOINPS D i am i 11 0-1 5-11 y 11 r ox y p h en a n t h r a n ap 11 t 11 az i n c-13-s u 1 p h o n i c C,,H,,ON,S l - P l i en yl-5-in e t 11 y l b enz o t h iazol e-4-az 0-8-11 apli t h 01 (MORGAN C2,H,,0,S2Si2 D i b en 1; y 1 d i e t 11 y 1 d i p r o p y 1 s il i c o e t h a n e d i s u I p h o 11 i c acid, (BARNETT and COOK) 911. XETT and Coos) 904. NETT and COOK) 905. of ( UAHNETT and COOK) 906. (BURROWS and TURSER) 435. and TURNER) 436. of (BURROWS and TuRNE~:) 435. P 11 e n y1-a-n a p h t 11 y 1 b c nz y 1 me t h y 1 a rs o 11 i u m 24 IV a c i d s (WATSON and DUTT) 1218.and WECSTEK) 1073. Z-nianthjlamine salt (KIIJPISG) 652. Czs Group. C2,H,,0a C25fl,,0N D i a c a t y l dcrirative of p h e n o l c o u m a r e i n (KRISHNA) 1423. 8-D im e t li y l a m i no-ll-pheuyl-&nap h t h a x a ‘1 t h Jn (KR:SHVA aiid 25 I11 POPE) 285. C,,H,,O,As H om op i p e r o n y 1 p h e n y l-a-n a p h t h y l In e t I i y 1 a r s o n i ti .n C,,H,,02Na C i n n a m y 1 i cl en eb i sp h en y I a c e t a in id e (Gum A) 301. C,,Ha50N3 4’-D i m e t h y 1 am i n 0-2-11 y d r o xy d i s t y r y 1 k e t o n e p h e n yl h yd r-C25H2e05Nz p h e n y 1-hydroxide salts of (BURROWS and TURNER) 434. azone (HEILBHON and BUCK) 1519. h y draz o n e (NIEItEh’STEIN) 167. 4:6:3’:4’-‘l’e t r am e t 11 o xy-3-ph e n y 1 chroma n-2-011 e 25 IV C,,H,,OBPAS C25H2202B~As P 11 e iiac y 1 p h en yl-a-iia p h t h y 1 xu e t h y l a r s o n i u ni H o m o p i p e r on y l p l i e n yl-a-nap li tli y l m e tli y l a r s o n i u i n b r o ni i dc (UURKOWS and TUILNE~:) 434.b r o m i d e (BURROWS and TURNER) 434. Cza Group. C2sH,,S Dibenzyl t h i a n t h r c i i (RAY) 1965. C3,,H21N 9-Di p h e n y 1 amino-9:lO-d ill y d r o a n t h ra cen e (DAENETI‘ and COOS), 912. C2sH,,N 9-y-R c n z c n e nz o pli en y 1 am in o-9:lO-d i 11 y d r o a n t h r B C e n e (BAR NETT and COOK) 911. 21 8’ 26 111-32 I11 FORMULA INDEX. 26 I11 C26HI,06N4 D i a n i l i d e of y-6:6‘-dinitrodiphenic a c i d (KENSEB and C,,H,,N,S, C,,Hz,ON, C26H&Nz STUBBINGS) 599. 3:6-D i t h i 0-1:2:4:5-t e t r a ph en y 1 h e Y a h y d r 0-1 :2:4:5te t r a z i n e 4’-D im e t h y 1 amino-2-m e t hoxgdis t y r g l (NAlK) 1169.ph en y l -hydrazone and its pyridine additive compound (HEILBRON and BUCK) 1520. ( FORSTER and SAVILLE) 795. k e t o lie Camp h or J’ 1 amino p h e n y 1 i m i n o camphor 26 IV Cz6H,,02N2S3 Tr i s u l p h i d o b i s b enzan il i d e (NAIK) 1169. C,,H,,O,N,S Be nz e n e-l:3-di sulp h o n y l bi s-1:4-n a p h t h y l e n c d i am i n e C26H,20,N,S2 29-D is m i n o p li e 11 a 11 t h ra q u i n o n edi ph e n y 1 h y d r a z on e-2qf-d i-(~IORGAN and GRIST) 606. sulphonic a c i d (WATSON and DUI’T) 1221. C,,H,,O,N,S p-S u l p h o be n z en e a z o n apli t h yl am i n o c amp h o r (FORSTER. and SAVILLE) $97. C.7f Group.C,,H,,O,CI Lac t one of 7:s-dib euzo y loxy-2:4-bis t r i c hlorom e t h yl-6.B-t r i c h 1 or o-a-h y d r o x y e t 11 y 1-1 :3-b e n z d i o x i n e-5-c a r b ox y 1 i c a c i d ( ALI 31-UHANUANI and &fELDUUM) 207. Czs Group. C2,HZ2O, C,,H,,O,N (KRISIIXA Cz,H,,N4C1 2:7-D inm i n 0-11 :4’-di m e t h y 1 f 1 a v i nrl u l i n e c h 1 or i d e ( WArso~ C,,H,,O,N Te t r a-a c e t y 1 derivative of 2:T-d i a m i n o d i h y d r o p h e n a n t h r a-1 :7:1’:7-T e t r a-ac e t o x y d i n a I ~ h t h y 1 (MORGAN and VINIXG) 17 13. 28 111 6-D i m e t h y 1 a m i n o-3-b en z o y 1 o s y-9-p h e n p 1 xan t h en alid POPE) 388. and DUTT) 1219. phenazine (WATSON and DUTT) 1217. 28 IV C,,Hl,O,N,C1 2:7-D i n i t r o-l1:4’-d im e t 11 y 1 f l a v i n d u l i n e c h 1 or i d e (WATSON and Duyr) 1218.Group. C,,H,,O,N Cam ph or y 1-1 -amino n a p h t h y 1-44 m i n oc a m p h o r (FowrEn and QAVILLE) 298. 30 1V C,H,404N4S N a ph t h a1 e n e d i s u 1 p h o n y 1 b i s-1:4-n a p h t h a1 e n e d i a m i n e s (MORGAN and GRIST). 606. CsoH;GON,I C i 11 n a 1x1 o y‘i a m i n 0-1 :l’-di rn e t 11 y lisoc y an i n c i od i de s (HAMER), 1440. Cal Group. C31Hza06 Dibenzoyl derivative of p h e u o l c i t r a c o n e i n ( I ~ I S I I K A and POPE), 290. CS2 Group. C88Hs,0,N3 pp’-B i s im i n o ca m p h o r d i ph en ylam i n e ( U . K. and M. SINGH and LAL) 1975. C3zH,o02N2 pp’-Diphenylenebisaminocamphor (B. I<. and M. SINCSH and LAL) 1974. 218 FORMULA INDEX. 32 IV-48 111 32 IV C32H3,0QNQS2 31 e t h y 1 ma1 on a n il i d e d i s u l p h i d e ( NAIR) 384. CS4 Group. C,,H,,O S u b s t ancp from magnesium phenyl bromide and dip?ienylchloro-34 111 C34H,,0aN2 oo’-Ditolylenebisini inocamplior (B. K. and 11. SINGH and C3,H,,04N 00’-D i m e t 11 ox y d i p h e n y 1 e n e b i s i ni i n o cam p 11 or (B. I<. and &I. acetyl chloride (SICKENZIE and BOYLE) 1138. LAL) 1973. SIKGH and LAL) 1974. 34 IV C3& 01,N6S P h en a n t h r a qu i n o n e b i s-(2’)-a zo-7’-a ni i n o-1’-h y d r o x J- n a p h-C,,H3,0,N,S3 Ma1 o n d i ni e t h y l a n i 1 i d e d i s II 1 p h i d e ( NAIIC) 384. thalene-3’-sulphonic a c i d s (WATSON and DUTT) 1219. CS6 Group. c3sEi2,0,8N,6S D odec a n i t r o-derivative of C36H3s0,N4S, m e t h ylm alono-p-t olu id i de disulphiiie (NAIK) 1238. Me thylmalono t o l u i d i d e d i s u l p h i d es (NAIIi) 1238. Cqo Group. C,,H,,08N,S2 C,,H,,O,N,S,. D i h y d r o p h e n an t h r a ph e n az i n e-2:7-bis-(2‘)-a z o n a p 11 t h i-11-Am i n oph en a n t l i r ap h enaz i ne-2:7-bis-(2‘)-az o-7’-am i n O-1’-hy d 1’0 x y n ap h t h a leu e-3‘-s u 1 p h o nic a c i d (WATSON and DUTT) 1220. onic a c i d (WATSON and DUTT) 1220. Ca2 Group. C4,H3,0 T r i b e ii zo y l derivative of pheno 1 c ou m a r e i n (KRISHSA) 1423. C4* Group. CQ4H2,0,,N,, CQ,H4,02N pp-D i p h e n y 1 e ne bi sa z oph e n y 1 amino c am p h or ( FOESTER and D i n a p h t h a-1 i:1’:7’-d i q u i n o n e t e t r a-2:4-di n i t ro p h e n y 1-hydrazone (MORGAN and VINING) 1712. SAVILLE) 797. C4* Group. C,,H,,OSi, C,,H,,O,Si O c t a p h e u y l s i l i c o t e t r a n e oxide rhomboidal (KIPPING and C,sH,,12Si Octaplienylcii-iodosilicotetrane (I~IPPISG and SANDS) 830. O c t a p h e n y l s i l i c o t e t r a n e oxide (KIPPING and Saxns) 840. SANDS) 844. 218

ISSN:0368-1645    

DOI:10.1039/CT9211902155

出版商:RSC    

年代:1921

数据来源: RSC

摘要:

ERRATA. VOL. 115 (TRAM. 1919). Pap Line 1386 6* for “latter” rcad “heat of formation of methnne.” VOL. 117 (TEAKS. 1920). Pagf Ppge Line { I ‘ 5 ’74 ”) { ( ‘ 57 :4 ” ) 5.15 51.5 I 56 Table V i n third columiifor 6’62 read 66 2 83 1* for ‘ I C,H,,O,N,S ” read “ C,€I,o~,N2S.” 345 21* , “ oxide a little water ” read oxide and a little water.” 348 6* , “citronella1 ” road “ citronellol.” 350 2 “ pzonal ” read ‘( pzono1. ” 475 13 , “ s ” read ‘( S.” 475 11 , “9r)s”mxd “9r)S.” , (‘0.15 cni.” read “0’1588 cm.” 476 15 4 i 8 10 ,) “6*69” rend “G*69 x 19.4.” 646 26 , “Mr. E. A. Perren” read “Nessra. R. Crsvcn and E. A. Perren.” 846 27 , “ h i s ” rend “tlieir.” 648 17 , ‘‘ AT/lO-KMnO,” rend “ N/10.1iMn04 equivalent to.’’ 648 20 , (‘ 0’03994 ” remi “,?‘03004.” 661 12 , ‘(sodium siilpliate read (‘ sodium hydrogen sulphatc.” 832 6 , “lend acetate” wad “sodium plumbite.” 965 h.leO/\CO,H McO<)CO,H , formukc V.and TI. read Me01 ’ \/ and Ho\/ OMc OMe respcctivclg. 1024 6* , (‘positive” rend “negative.” 1026 16* the formnla should be (‘ 3K3~Fe(C~~,],h‘,[~e(CN)SII,0].” 1218 19 col. 2 for “ 167*90” read “ 157.90. 1219 1270 7* .for “ C,,H,,O,N ” read “ C,,H,20,N,. 1276 22 , “B=17.37. C1,HItO6N requires N=17*i3” rend 1560 4* , “2,S” rend “28.” 1660 ,13* , “ 2 8 ” read “2B.:: 1560 15* , “28 ” yead “ 2 8 . diagram insert “ y ” values at elid of horizontal lines namely from below upwards “ 100 90 80 70 !O.” 1\7 = 16 ‘35. C20H1g0,N5 requires N=16*47.” VOL. 119 (TRANS. 1921). i: 50 14 , “SrCS,,SH,O” wad “SrCSo,8Hz0.” 63 4 , ‘‘salts i u niillimolu.” read “salts and soaps in millimols. per ccnt.” i n labIcs I 11 V VI and VIII after “millimols.” iizsert “per cent.” , “S1ienstone 9’ read ‘(~ten~ionse.” 66 68 15 f o r ‘‘ renewal ” rend ‘( rerersal.” 2190 * From bottoni ERRATA (continaed). VOL. 119 (TRAM. 1921). Page Line 307 389 8* , ( ‘ cis. Citmcomtodiethylenediainine ‘I read cis-Citraconatodi-for “denominator of equation ” read “ 4( Vo)l - (Yf + &).I’ et hit Zenedianainecobal tic. ” In equation; ( 6 ) (7) (8) and in tables 11 111 IV for c‘log,’y read 1392 “ 10,010. 1590‘ 11 for “ ay-dicarboxy-a-methylglutaconate ” read (‘ ay-dicarboxy-a-1735 14 , ‘‘ (CllHloO,),Ca” read “ (C1lH,O,),Ca.” benzylglutaconate. ” * From bottom. 219

ISSN:0368-1645    

DOI:10.1039/CT9211902190

出版商:RSC    

年代:1921

数据来源: RSC