FORMULA INDEX. THE following index of organic cornpounds of known empirical formula is arranged according to Richter’s system (see Lexikon der Kohlensstofl- Verbhdungen). The elements are given in the order C €I 0 N C1 Br I F S P and the remainder alphabetically. The compounds are arranged-Firstly in groups according to the number of carbon atoms (thus C group, C group etc.). Secondly according to the number of other elements besides carbon contained in the molecule (thus 5 IV indicates that the molecule contains five carbon atoms and four other elements). Thirdly according to the nature of the elements present in the niolecule (given in the above order). Fourthly according to the number of atoms of each single element (except carbon) present in the molecule. Salts arc 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 Me thane ignition of mixtures of air and (MASON and WHEELER) 36 122T ; (WHEELER) 903 ; propagation of flame in mixtures of oxygen nitrogen and (PAYMAN) 48 ; action of chlorine with under the influence of light (WHISTON), 183. COa Carbon dioxide pure preparation of (FARNER) 1446. CHN Hydrocyanic acid mercuric salt action of on metallic salts (GUPTA), CH,C1 Methyl chloride conversion of into methyl alcohol and methyl CH40 Me t h y 1 alcohol synthesis of froin methyl chloride (WHISTON) 183. CH,N Me t h y 1 am i n e preparation of from ammonium methyl sulphate (DENHAY CH,N Guanidine preparation of (WERNER and BELL) 1133.(;O,N T e t r a n i t r o me t h a n e preparation and properties of (ORTON and McKIE), 294; effect of reducing agents on and a rapid method of its estimation (BAILLIE MACBETH and MAXWELL) 880. 1 I1 67 ; nickel salt preparation of (GUPTA) 69. acetate (WHISTON) 183. and KNAPP) 236. 1 111 CHON Cyanic acid constitution of and the formation of urea from its CHO,N N i troform estimation of with potassium permanganate (McI~IE) 646. CHNS Thiocyanic acid metallic salts compounds of hydrazine with (RAY and SARKAR) 321 ; ammoiiiuni salt interaction of dicyanodiamide and (WERNER and BELL) 1133. interaction with animonia (WERNER arid FEARON) 1356. CH,O,N GII,ON . Carbamide mechanism of the synthesis of (WERNER) 1046 ; decom-COC1 Carbonyl chloride preparation and physical properties of (ATKINSON, Methyl n i t r i t e preparation of (SLATEB) 588.position of (WERNER) 1078. HEYCOCK and POPE) 1410. Cz Group. C,H1 Acetylene action of nitric acid on (OXTON and McKIE) 283. C,H4 E t h y 1 en e interaction of selenium chloride and (BAUSOR GIBSON and POPE), 1453. 166 FOltMULd INDEX. 2 11-4 111 2 I1 C,H,N, C,HJ C,H,O D i c y a n o d i amid e interaction of ammonium thiocyanate and (WERNER and BELL) 1133. E t h y 1 i o d i d e preparation of (HUNT) 1592. E t h y l a l c o h o l surface tension of mixtiires of water and (Fmrn) 268 ; equilibrium in the system benzene water arid (SIDGWICK and SPURRELL), 1397 ; action of on sodium sulphates (BUTLER and DUNNICLIFF) 649.C2H,N2 C,H,Te M e t h y l t e l l u r i d e (VERSON) 892. C2H,0,C1 C2H,0C1 C,H,OBr C,H,Cl,As E t h y 1 d i c hl o r o a r s i n e (MCKENZIE and WOOD) 407. C,H,OT€! C,H,O,Te D i m e t h y 1 t e 11 u r o n e preparation of (VERNON) 894. C,H,CI,T0 Dime t h y l t e l l u r o n i u m d i c h l o r i des (VERNON) 98. C,H,Br,Te D i m e t h y l t e l l n r o n i u m dibromides (VERNON) 96. CzHeIAS C,H,I,Te C,H,ON, 759. C,H,O,Te Dime t h y 1 t e l l u r o n i u m d i l l y d r o x i d e (VERNON) 897. 2 I V C2H50C1,As E t h o x y d i c h l o r o a r s i n e (MCKENZIE and WOOD) 406. a-Amino-a-iminoethane and its salts (FARGHER) 674. 2 I11 C h 1 o r o a c e t i c a c i d preparation of esters of by means of aB-dichloro-C l i l o r o m e t h y l e t h e r syntheses by means of (SIMONSEX) 564.E t l i y l e n e b r o i n o h y d r i n preparation and characterisation of (READ vinyl ethyl ether (CROMPTON and VAKDERSTICHELE) 691. and HOOK) 1214. D i r n e t h y l t e l l u r o n i u m o x i d e and itssilver salt(VERNoN) 94 889. D i m c t h y l i o d o a r s i n e preparation of (BURROWS and TURNER) 1376. Dime t h y 1 t e l l u r o n i u m di-iodide s (VERKON) 90. Matliylsemicarbazides and their oxalates (FORSTE~L and SAVILLE), Ct Group. C3H404 C,H,N, C3H,02 3 I11 C,H,ON Cyan o a c e t a m i d e condensation of aldehydes with (DAY and THORPE), C,H,O,Cl E t h y l c h l o r o f o r m a t e action of pyridine and quinoline with C,H,ITe Ma 1 o n i c acid rate of decomposition of ( HINSHELWOOD) 156. Aminoglyoxaline dipicrate of (FARGHER) 673.M e t h y l a c e t a t e synthesis of from methyl chloride (WEISTON) 183. 1465. (HOPKINR) 278, T r i m e t h y l t e l l u r o n i u m iodide preparation of (VERNON) 894. 3 I V C,H,O,N,S 1430. G l y o x a l i n e s u l p h o n i c acid and its salts (PYMAN and RAVALD), Ca Group. C4H,0 r - T a r t a r i c a c i d resolution of by means of Z-borneol (WEEN WILLIAMS, C4H7N3 -4-Am ino-5-me t h y l g l y ox aline and its salts (FAKGIIER) 675. C4H,0 n-B u t a 1 d e h y d e condensations of ( WEIZMANN and GARRARD) 324. C4HI0O n-B u t y 1 a1 c o h 01 condensations of ( WEIZMANN and GARRARD) 324. C,H,,N D i e t h p l e n e t r i a m i n e and its salts (FARGHEB) 1351. C,H,OC1, and MYDDLE~ON) 191. 4 111 aB-Dichlorovinyl e t h y l e t h e r preparation of and its synthetic uses (CI~OMPTON and VANDERSTICHELE) 691.166 4 111-0 I1 FORBiULA INDEX. C4H,C1,S BB’-Dichlorodie t h y l s u l p h i d e (GIBBON and POPE) 271 ; syntheses C4H,Cl,Se BB’-D i c h l o r o e t h y l s e len i d e d ich 1 o r i d e ( BAZTYOR GIBSON and C4HsNS l:4-Thiazaii and its salts (UAVIES) 306. C,H,,O,Te C4H1,NI Tetramethylanimoniumn iodide mercuri-iodide of and its ci.yatallo-with (DAVIES) 297 ; estimation of volnmetrically (HOLLELY) 895. POPE) 1454. Dime t h y 1 t e l l u r oni uin dime t 11 oxide (VERNON) 897. graphy (BARKER and PORTER) 1312. 4 IV C4HsOCl,S BB’-Dichloroe t h yl s n l p h o x i d e (GIBSON and POPE) 277. C,H,O,N,S Car b o me t h o x y-$-t h i o c a r b a m i d e C4HloOzC1As D i e t h ox y c h l o r o a r s i n e (MCKENZIE and WOOD) 407.C4H,0aN,C1,S T h i o ca r ba m i d e met 11 y 1 t r i c h 1 o ro 8 c e t a t e (TAYLOR) 10. C4H,OaN,C1,S T h ioc a r ba rn i d e in e t h y 1 ct i c h l o r o a c e t a t e (TAYLOR) 10. C,H,O,N,ClS Me t h y 1 isot h i o h y d a n t o a t e 11 y d r o c h 1 o r i d e (TAYLOR) 9. CaH1,ON4C1,Co trans-D i c hlo r o d i e t h y 1 en e diainine c obal t i c h y d r o x i d e, bicarb 011 ate (Drsoiv and KENNEDY) 85. 4 v Thiocarbamide me t h y l c h l o r o a c e t a t e (‘~’AYLoR) 7. salts of (PRICE and DUFF) 1076. Ca Group. C&N P y r i d i n e action of ethyl chloroformate on (HOPKINS) 278. 5 111 C,H,O,Te T e l l u r i u m s c e t y l a c e t o n e (MORGAN and DREW) 1461. CsHs02C1 n - B u t y l chlorofor mate (CHATTAWAY and SAERENS) 708.C6H,,0aN rt-Butyl carbamate (CHATTAWAY and SAERENS) 709. 5 IV C,H,O,Cl,Te T e l l u r i u m ace t y l a c e t o n e d i c h l o r i d e (MORGAN and DERW), 1462. C&,O,N,S Carbomethoxyiso t l i i o h y d a n t o i u (DIXON aiid KENNEDY) 79. C6H804NBS D i c a r b o m e t h o x y t h i o c a r bamide ( D r x o ~ and KENNEDY) 85. CsH,,O,NzS C a r b e t ho x y-q-t h i o c a r ba ni ide CsH,,OpNaCIS C,H1,0,N4SaC~ cis-M e t h i o n a t o d i e t h y 1 en e d i am i n e c o b a1 t i c h y d r o x i e, 5 v b i c a P b o iia t e ( D r x o ~ and LENNEDY) 83. T h io c a r barn i d e e t h y 1 c h 1 or o ac e t a t e (TAYLOR) 10. salts of (PRICE and DUFF) 1073. 5 VI C,H,,O,N,BrS,Co cis-M e t hio n a t o d i e t h y 1 e n e d i a 111 i n e c o bal t i c bro m i d e ( + 2H,O) (PRICE and DUFF) 1073.Cs Group. c,H Benzene influence of drying agents on the freezing point of (SIIIGWICK), 1340 ; equilibrium in the systeiii ethyl alcohol water and (SIDGIVICK and SPURRELL) 1397. 6 I1 C6Hl,0 E t h y l ace toace t a t e condensation of with p-diniethylaminolenz-C,H& C,H1,O, C6H,,S T r i e t h y l e n e t r i s u l p h i d e (RAY) 1090. aldehyde and ammonia (HINKEL and CREMER) 137. Methyl n - b u t y l c a r b o n a t e (CHATTAWAY and HAEHENS) 709. Fructose relationship of inulin to (IRVINE and STEELE) 1474. G 1 u c 0s e conversion of cellulose into ( IRVINE and SOUTAK) 1489. 166 FORMULA INDEX. 6 11-7 111 CaH12S T r i e t h y l e n c t e t r a s u l p h i d e s (RAY) 1090.C,H,,S T r i e t h y l e n e d i s u l p h i d e d i m e r c a p t a n (RAY) 1092. C,H,,N T r i e t h y l e n e t e t r a m i n e and its salts (FMLGEKER) 1354. 6 I11 C,H,I,As P h e n y l d i - i o d o a r s i n e (BURROWS and TURKER) 1376. C,H,ON Ar-Ni t r oso-8-p h e n y 1 h y d r o x y l am iiie ammouium salt (cupferron), C,H,O,N N i t r o p a e n o 1 preparation of ( REKNIE COOICE and FINLAYSON) 342. C,H,,O,N, C,H,O,N,B N i t r o s o b o r a n i l i d e (CHAUDHURK) 1082. C,H,ONB C,H,NSB C,H,O,N,S C,H12C1,S,Hg, C,Hl,NIS C,H,ONBrB B r o m o b o r a n i l i d e s (CHAUDHURI) 1082. C,H!,O,N,SCo preparation of (SLATE~L) 591. M e t h yl a in in o n i 11 m d i e t h y l c a r b am a t e (WERNER) 1052. 6 I V B o r s n i l i d e and its salts (CHAUDHURI) 1032.Th i obo r a n i litle (CHAUDHURI) 1083. C a r b e t h ox y iso t h i o 11 y d a 11 t o i n and its liyiirochloricie (DIXOX D i c h l oromercap t i d e from triethylene disulp'hide dinicrcaptan and KESNEDY) 75. and mercuric chloride (RAY) 1092. 1:4-Thinzan e t h i o d i d e (DAVIES) 308. 6 V cis-S u l p h o a c e t a t o d i e t h y i e n e d i a m i n e c o b a1 t i c h y d r o x. i d e salts of (PRICE and DUFF) 1072. 6 VI C,HI,,O,N,BrSCo cis-Su 1 p 1-1 o a c e t a t o d i e t h y1 e n e d i a in i n e c o b a1 t i c b r o m-i d e (PILICE and DUFF) 1072. C Group. C7H13 H e p t a d i e n e froin n-butyl alcohol acetone and aluminium oxide ( WEIZ-C7H14 H y d r oc a r b o n from n-butvl alcohol acetone and aluniiuium oxide MANX and GARRARD) 337.(WEIZMANN and GARRARD) 337. ' 7 I1 C7H,Br6 P e n t a b r o r n o b e n z y l b r o m i d e (DHAR) 996. C,H,02 C,Hs02 C7H9N C,Hl,Oa cyelo-Pen t y l i d e n e a c e t i c a c i d (BECKER and THORPE) 1582. C7H1004 tram-Caronic acid preparation of and its silver salt (SKYOXSEX), C,H,,O AY-Heptylene-B-one (WEIzmm and GARRARD) 335. C,H,,O aa-D ih y d r ox y-BB-d i m e t h y 1 g 1 u t a r i c a c i d preparation of (FARMER C,H,,O E t h y l n - b u t y l c a r b o n a t e (CHATTAWAY aud SBEREKS) 709. 7 I11 C,H,OBr, C,H,O,N 2:3:6-Trinitrotoluene preparation of (DBEw) 1615 ; synthesis of B e n z o i c a c i d volatility of and its derivatives in steam (SIDGWICR), G u a i a c o 1 arsinic acids derived from (FARGHER) 865. 396. Me t h y l a n i l i n e cadmi- and cobalto-chlorides of (REILLY and HICKIN-BOTTOM) 130.577 ; (FARMER and INGOLD) 1372. S u b e r on e preparation of (DAY KON and STEVESSON) 642. *and INGOLD) 1371. P e n t a b r o mo b e n z y l a l c o h o 1 (DHAR) 997. (ERADY and TATLOE) 876. T r i n i t r o t o 1 u c n e s preparation of (BILADY and WILLIAMS) 1137. CXVI I. 1665 3 7 111-8 11 FORMULA INDEX. C7H508N T r i n i t r o p h r n y lm e t h y l n i t roamin e (tetryl) velocity of decompo-hilion of (FARMER) 1603 ; action of ainines on (JAMES JONES and LEWIS), 1273. C7H,0,N D i n i t r o t o l u e n e s preparation of (BILADY and WILLIAMS) 1137 ; action of ammonia and sodium methoxide on (KENNER and PARKIN) 852. 3-Ni t r o a n t h r a n i l i c acid preparation of (JAMES KENNER and STUBBINGS), 775.C,H,O,N 2:6-D i n i t r o-m-cr e s o 1 (DREW) 1618. C7H,0,N4 2:4:5-Trini t rom e t h y l a n i l i ne (SWANN) 3. C7H,N,C1 C h l o ro t o 1 y l e n e diazoi mines (MOHGAN and DREW) 789. C7H70,N 5:6-Dinitro-o-toluidiiie (BRAUY and TAYLOK) 879. D i n i t r o t o 1 u i d i n e s preparation and separation of ( BRADY and WILLIAMS), 1138. C7H8C1As C,H,IAs Phenylmethyliodoarsine preparation of (BURROWS and TURNER), 1377. C7Hs05As H y d r ox y m e t h o xy p h en y 1 a r s i n i c acid s and their calcium salts (FABGHEB) 872. C7HsN,C1 C h l o r o t olylen ediam i n e s (MORGAN and DP.EW) 786. C,H,,NI Methyltriethylammonium iodide mercuri-iodide of and its 7 IV P h e n y 1 met h y l chlor o a r s i n e (Bun~.ows and TURYER) 1377. crystallography (BARKER and PORTER) 1313.C7H,0zN,C1 C7H404NI 2-1 o d o-3-n i t r o b c n z o i c acid preparation of (JAMES KENNER and STUBBINGS) 776. C7H502NBr2 D i br o m o h y d r ox y b enz nld ox i m es ( WENTWORTII and BRADY), 1042. C7H504N2C1 C h l o ro d i n i t r o t 01 ue n es (MORGAN and DREW) 786. C7H7O,N,Cl C h l o r on i t r o t o l u i d i n es (MORGAN and DREW) 787. C,H,O,NAS 3-Nitro-4-niethoxyphenylarsinic acid and its sodium salt (FAHGHER) 868. C,H,O,NAs N i t r o h y d r o x y m e t h o x y p h e n y l a r s i n i c a c i d s (FARGHER), 871. C,H,o04NA~ 3-Axnino-4-m e t h ox y p h e n y 1 a r si n i c acid (FARGHER) 869. C7H1204N,S D i c a r be t h oxy t h i o c a r bamid e (DIXON and KENNEDY) 83. 7 V C7H,O2NC1I 5-Chloro-4-iodo-3-nitrotoluerle (JAMES KENNER and STUBBLNGS), C,HIsO4N4BrCo cis-M a l o n a t o d i e t h y l e n e d iam i n eco b a1 t i c b r o mid e (PKICE 4-C h l o ro-7-n i t r o i n dazole (MORGAN and DREW) 787.776. and DUFF) 1076. C Group. C,H,O, CeH60s Lac t o ne An h y d r o-a c i d s from c a r b ox ym e t h a n e-1113-3-m e t h y 1 cycckopr o-pane-l:2-dicarboxylic a c i d s (BEESLEY and THORPE) 613. h y d r o x y c a r b o x y m e t han e-II1:3-3-m e t h y IczJcZopr o-pane-l:2-dicarboxylic a c i d (BEESLEY aud THORPE) 616. Met h y 1 met h a n e-III1:2:3-cyccko p r o p a n e-1:2:3- t r i c a r b o xy 1 i c acid and its silver salt (BEESLEY and THORPE) 617. T r i-la c t o n e of afl8-t r i h y d r o x y d im e t h y 1 p r o p a n e t r i c a r b ox y 1 i c acid, and its silver salt (BEESLEY and THORPE) 618.C,H7C1 3:5:6-Trichloro-o-xylen e (HINKEL) 1300. C,H,O, of F i s e t 01 (w-hydroxzJ~esaceto~~e~o~e) synthesis of derivatives of (SLATER and STEPHEN) 309. 166 FORMULA INDEX. 8 II-8 IV C,H,04 Phloroacetophenone (SEN and GHOSH) 61. csH,o8. C a r b ox y me t h a n e-IIlt3-3-rne t h y 1 cycZop r op a n e-l:2-d i c arbo x y 1 i c gs-dihy d r o x y d im e t h y 1 p r o p a n e t r i c a r b oxy li c acid a c i d s and their salts (BEEBLEY and THORPE) 612. (BEESLEY and THORPE) 612. D i l ac t o ne of C,H,Cl 2:w(4)-Dichloro-p-xylene (STEPHEN SHORT and GLADDING) 524. CsH8C15 2:3:3:4:5-Pen t a ch 1 o r o-1:l-di m e t h y l-A5-cycZo h e x ene (HINKEL) 1299. C8HloOa Vera t r o 1 e arsitiic acids derived from ( FARGHER) 865. CsHloC12 35-D i c h l o ro-1:l-dim e t h yl-A2:4-cycloh e x a d i e ne action of chlorine C,H,,As P h e n y I d i me t h y 1 arsine prepar‘ttion of (BURROW and TURNER), C8H1203 B - P r o p y l g l u t a r i c a n h y d r i d e (DAY and THORPE) 1472.CsH,,08 8B-D i h y d r o x y d i me t h y l p r o p a n e t r i c a r b o x y 1 ic acid and its silver C,H,,O CsH1404 8 - P r o p y l g l u t a r i c acid andits silver salt (DAY and THOILPE) 1471. C,H1,02 a-E t h y l h e x o i c acid preparation of (WEIzhrANK and GARRARD) 330. C,H,,O n-Propyl w b u t y l c a r b o n a t e (CHATTAWAY and SAERENS) 709. C,H,,O a-E t h y 1 h ex y 1 a 1 c o h o 1 preparation of (WEIZMANN and GARRARD), 329. on ( HINKEL) 1296. 1378. salt (BEESLEY and THOI~PE) 612. a-Ethyl-Aa-h exenealdehyde (WEILMANN and GARRARD) 329.S u b e r i c acid preparation of (DAY KON and STEVENSON) 641. 8 I11 C8H,041 2-1 o d oiso p h t h a1 i c a c i cl preparation of (JAMEB KENNER and STUBBINGS) 774. C,H,O,Br Brom o-an h y d r o-acid from brom oca r bo x y m e t h ane-111:s-3-me t h y lcyclopr opane-l:a-di c a r bo x y l i c a c i d ( BEESLEY and THORPE), 615. C,H,Cl,Br C,H,O,Br. Bro m oc arbo xyme t hane-I11:3-3-m e t h y lcyclo p r opan e-l:2-dicarb-C8Ha0,N 2:6-Dinitro-m-tolyl m e t h y l e t h e r ( D e ~ w ) 1618. C8H,03N3 3-C y ano-2:6-d i k e t o-4-m e t h y l p i p eridine-5-car box y l a mi de (DAY C8H,04N3 a- and B-D i n i t r o d i m e t 11 y l a n i l i n es ( SWANN) 2. C,H,,02N4 aa’-Di c y a n o-8-m e t 11 y 1 g l u t a r a ni i d e C,H,,O,N 4-Ami noveratrole preparation of (FARGHER) 869.C,H,,O,As 3:4-Dim e t ho x y p h e n y l a r s i n i c acid (FARCHER) 870. C,HlaN2S2 N i t r i 1 e from potassium cyanide and BB’-dichlorodiethyl sulphide C,H,,O,S y-Thiodibuty r i c a c i d (DAVIES) 301. C,H1404S Acid from hydrolysis of nitrile C,TT12N,S2 (DAVIES) 305. C,HI,ON AY-Heptylene-&one semicarba zone (WEIZMANN and CARRARD), 335. C,H2,NI T e t r a e thylammonium iodide niercuri-iodides of and their crystal-lography (BARKER and PORTER) 1313. 3:4:5-Tric hloro-6-bromo-o-xyl en e (HIXKEL) 1300. o x y l i c acids (BEESLEY and THORPE) 615. and THORYE) 1470. and 6-1 111 i n o-3-c y a n 0-5-c a r ba myl-4-m e t h y 1-%pi per id one (DAY and TIIOR~JE) 1469. ( DAVIES) 305. 8 IV C,H,0,NC13 3:4:5-Tr i ch l o r o-6-n i t ro-o-x y 1 en e (HINKEL) 1301.C8H802NC1 C h l o r o n i t r o x y l e n e s (STEPHEN SHORT and GLADDING) 524. C,H,02NBr 5-Bromo-o-me t h oxy benzaldoxime and its hydrochloride (WENT-C,H,,OClAs P h en y 1 e t h o x y c h l o r o a r s i n e (Mc KENZIE and WOOD) 410. WORTH and BRADY) 1043. 166’ 8 IV-9 I11 FORMULA INDEX. C,H,,O,NAS C,H1206NAs 5-N i tro-3:4-di m e t h o xyp h e n y l a r (I i n i c a c i d, 5-Am i n o-3:4-di m e t h ox y p h e n y l a r s i n i c a c i d (FARGHER) 871. and its salts (FARGHER) 870. C9 Group. C,H,N C9Hs02 C,Hlo03 Quinoline action of ethyl chloroformate on (HOPKINS) 278. Methylcoumaranoiies preparation of (HIGGINBOTHAM and STEPHEN), Mandelic acid racemisation of esters of ( M C ~ N Z I E and WREN) 685. 1541.T o l y l o x y a c e t i c acids preparation of and their salts (HIGGINBOTHAM aud STEPHEN) 1534. C9H100P 343. C,H1005 D i In e t h y ldicyclop e 11 t a non e d i c a r b ox y 1 i c (PARMER and INGOLD) 1371. S y r i n g i c a c i d (ALIMCHANDANI and MELDRUM) 967. 2:4:6-Trihydroxy-w-methoxyacetophenone (+ H,O) (SLATER and C,HI20 Lac t on e of a-h y d r ox y cydop e n t a n e-1 l - d i ace t i c a c i d (BECKER and cis- and trans-cyclo P e n t an espirocych p r o pan e-l:2-di car bo x y l i c acids and C,Hl,O L a c t o n i c a c i d of aa'-d i h y d r ox y cycclo p e n t a n e-l:l-di a c e t i c a c i d CsH12N2 as-Ph e n y 1 a l l y 1 h y d r a z i n e (SINGH) 1212. C,H13As P h e n y 1 m e t h y l e t h y l a rs i ne (BURROWS and TURNER) 1380. C9H1405 a-Hydroxycyclopen tane-1:l-diacetic acid silver salt (BECKER and C9ZI14N2 as-Phenyl-a-propylhydrazine and its hydroferrocyanide (SINGH), C9H1806 Trime t h y 1 y-fructose (IRVINE and STEELE) 1485.w-Nethoxyresacetophenone (SLATER and STEPHEN) 312. Substance from the resin of Xanthorrhcca (RENNIE COOKE and FIKLAYSON), of acid oxidation STEPHEN) 316. THORPE) 1586. the silver salt of the latter (BECKER and THORPE) 1587. (BECKER and THORPE) 1585. TRORPE) 1587. 1206. T r i m e t h y l glucose (HAWOETH) 207. 9 I11 C8H,03N C,H,O,N A c e t y l derivative of 2:4-dinitrobenzaldoxime (WESTWORTH and CsH,07N4 2:4:6-Tri n i t r oace t o-m-t oluidide (COOK and BRADY) 750. C,HsON T o l y l o x y a c e t o n i t r i l e s (HIGGINBOTHAM and STEPHEN) 1540. CoH,O,N 5-H ydr ox y-l-me t h ylcoumaran-2-011 e (SLATER and STEPHEN) 317.CSHgO2C1 To 1 y 1 ox yac e t y l c h l o r i d e s (HIGGINBOTHAM and STEPHEN) 1538. CsH805N D i n i t r o a c e t o-o-t o 1 u i d i d e s (BKADY and TAYLOR) 879. CsHllON p-D i m e t h y 1 a m i n o b e nzal d e h y de condensation of ethyl acetoscetato C,HI1O2N Tolyloxyacetamides (HIGGINBOTHAM and STEPHEN) 1539. COHI1O3N3 3-Cyan o-2:6-d i k e t o-4-e t h y 1 p i pe ri dine-5-car bo x y 1 a m i d e (DAY C,HllO,As Ace t 0 x yme t h o x y p h e n y 1 a r s i n i c a c i d s (FARGHER) 872. C8H1202N4 aa'-Dicyano-B-ethylglutaramide (DAY aiid THORPE) 1470. o-Nitrocinnamaldehyde preparation of (MILLS and EVANS) 1037. BRADY) 1042. D i n itroaceto-m-t o l u i d i d e s (COOK and BEADY) 752. and ammonia with (HINKEL and CREMEEL) 137.and THORPE) 1471. 6-1 m i n 0-3-c y an o-5-car b am y l-4-e t h y l-2-pi p e r i d one (DAY and THORPE), 1471. C8H1203S Mesi t y l e n e s u l p h o n i c acid preparatiou of (GIBSON) 949. 166 FORMULA INDEX. 9 Irr-io 11 C,H,,O,Br aa’-D i b r omo cyclop e n t a n e-1:l-d i a c e ti c a c i d (BECKER and CBHl,NI P h e n y 1 t r i m e t 11 y 1 a m m on inm i o d i de mercnri-iodide of and its C,Hl,I,As2~ Substance froni phenyldimethylarsine and methyldi-iodoarsine CsH170N2 Ph en y 1 me t h y 1 e t h y 1 a z o n i u m h y d r oxide s salts of and their C,H,,NI Triethyl-a-propylammonium iodide mercuri-iodide of and its 9 IV THORPE) 1585. crystallograpliy (BARKER and PORTER) 1316. (B,URROWS and ‘FURNEE) 1378. resolution (SINGH) 1204.crystallography (BARKEK and PORTER) 1314. CgH04NBr T e trabromo-6-nit r o c oum n r i n (DHAR) 1000. C,H,O,NBr T r i b r om o-6-n i t r o c o urn a r i n (DHAR) 1000. CsH304NBr 3:s-D i b r omo-6-ni t roc o umarin (DHAR) 1000. C,H,O,N,Br 3-Bro mo-6:s-dini t r o co u m a r i n (DHAR) 1000. C,H,O,NBr 5 - B r o m o v e r a t r o n i t r i l e (WENTWORTH and BRADY) 10.15. C,H,,O,NBr 5-Br o m o-3:4-di m e t h o x y b e nzald oxime s and C,Hl,07N,S Dinitro-+-cumene-5-sulphonic a c i d (+ 4H20) and its salts Dinitromesitylenesulphonic acid ( f 4H20) and its salts (GIBSOX) 950. CsH,,06N3S Din i tro-+-cum e n e-5-sul p h o n amid e (GIBSON) 955. D i n i t r omesi t y l e nes u l p hon am ide (GIBSON) 951. C,H,a0,N2S N i t r oam ino-+-cu men e-5-sul p h o n i c a c i d (GIBSON) 956.CSHl4O3N,S I) i aniino-+-cu mene-5-sulphonic acid (GIBSOS) 956. CgH2,0,N,Co ( WENTWOI~TH BKADY) 1044. (GIBSON) 953. D i am i n om e s i t y 1 en e s u l p h onic a c i d (GIBSON) 952. cis-11 i m e t h y 1 m sl on a t o d i e t h y 1 e n e d i a m i n e c o b a 1 t i c h y d r -oxide salts of (PRICE and DUFF) 1076. 9 v CgHg06N,C1S C,H,,O2N2C1S C,H2,O4N,C1Co C,H,,O,N,BrCo I) i n i t ro-$-cum ene-5-8 u l p h on y 1 c h I orid e (GIBSOX) 955. T h i o c a r b a m i d e be n z y 1 c h l o r o a c e t a t e (TAYLOR) 8. Din i t r o m e s i t y l e n e s u l p h on y 1 c h 1 or i d e (GIBSON) 950. &-Dime t h y l m a10 n a t o d i e t h y 1 en e d i am i n e co bal t i c c h l o r i d e (PEICE and DUFF) 1077. bromide (f 2H,O) (PRICE DUFF) 1077.ch-D i m e t h y 1 ma 1 o n a t o d i e t h y 1 en e d iain i ne c o bal t i c Clo Group. CIOHIB d-Carene (SIMoXsEx) 574. l-M e t hyl-3-iso p r o py 1-A4:6-cycZo1] ex a d i e n e ( HENDERSOPU’ and SmcArohT) 149. CloHl l - M e t h y l-3-isopr o py l-As-cycZoh ex en e (HENDERSOS and SMEATOS), 10 I1 148. C,,H,Br, CroH,Br, CIOH80G 4-Hy d roxy-3:b-dime t ho xyp h t h a l i c a n h y d r i d e (ALIMCHASDANI C,,H1,O a-B en z y l a c r y l i c a c i d (SIMONYEN) 567. C,,H,,O 4-H y d r o x y-35-d im e t h ox y p h t h a1 i d e (ALIMOHARDANI and MELD-C,H,OO7 4-Hy d r oxy-3:5-d i m e t h ox y p h t h a l i c acid (ALIMCHAKDANI and Hexa bromonap h t ha1 ene (DHAR) 997. Te t r abrom onap h t h s l e n e s (DHAR) 99T. and MELDRUM) 970. RUM) 969. MELDBUM) 970.166 10 I1 -10 I11 FORMULA INDEX. C,,]H,,O 3:4:5-Trimethoxyphtlialide preparation of (ALIMCHANDAKI and C,,H,,N o- and p-To 1 ue n e a x o g l y o x a l i n e s (PYMAN and RAVALD) 1426. C,,H,,N Di h y d ro-a-naphthylamines and their hydrochlorides (ROWE and MELDRUM) 969. LEVIN) 1576. C,,H,,O 3:4:5-Trimethoxybenzoic acid salts of (ALIMCIIANDAN; nnd CloHlzOs fib-D i h y d r o x y d i m e t h y 1 prop a n e c a r b e t h o x yd i c a r b o x y l i c a c id C,,H,,N 2:4’-D i am i n o-4-nz-t o 1 y l g 1 yo x a 1 i n e and its salts ( PYMAN atid C,,H,,Br C,,H,,O p-sec.-Bntylphenol preparation of (REILLY and HICKISBOTTOM) 122. MELDRUM) 967. d i l a c t o n e (BEESLEY and THORPE) 611. RAVALD) 1428. 4-Bromo-n-butylbenzene (RETLLY and HICRINBOTTOM) 112.4-Hydroxy-qt-butylbenzene (REILLY and HICKINBOTTOM) 114. 6-Hydroxy-m-isocymene (HENDERSON and SHEATON) 147. C,,H,,Oa 2:4-Dimetlioxyethylbenzene (NIEREKSTEIN) 973. C,,H,,N Amino-n- and -scc.-butylbenzenes and their salts (REILLY and n- and sec.-Butylanilines and their salts (REILLY and HICICINBOTTOXI) 121, C,,H,,As P h en y 1 d i e t h y 1 a r s i n e preparation of (BURROWS aud TURNER), C,,H,,N 4-n-Butyl-o-phenylenediamine (REILLY and HICKINBOTTOM) 118. C,,H,,O isoPulego1 physical properties of and of its esters (PICKARD HUXTER, C,,H,,O d-Ca r en e gl y c o 1 (SIMONSBN) 576. C,,H,,O 2-Hexylsuccinic a c i d (WREN atid BITENS) 266. C,,H,,Br 5:6-D i b r o m o-l-m e t hyl-3-isopr op y 1 cyclo h ex a n e (HENDERSON and SMEATON) 148. C,,H,,O l-Me t h y l-3-isopr op ylcycloh exan-6-01 (HENDERSON and SMEATON), 147.CloHzoOe T e t r a n i e t h y l f r u c t o s e s (HAWoKrH) 207 ; (XWINE and STEELE), 1488. HICKINBOTTOM) 110 126. 126. 1379. LEWCOCK and PENNIKGTON) 1248. 10 111 C1,H,O,N3 C,,H,O,N 1 :2:6:8-T e t r a n i t r o n a p 11 t h a1 e n e (DIIAR) 1004. C,,H@Na Sodium 8-naphthoxide action of alkyl iodides with (Cox), 493. C,,H,ON C,,H,,O,Br ab’-Di bro mo-8-ph en yliso bu t y r i c a c i d (SIMONSEN) 568. C,,H,,ON, C,,H,,O,Br B rom o-8-p heny liso b u t y r i c acids (SLMONSEN) 568. Cl,H,,O,N T r i 11 i t r OD hcnyl-n-bu t y l n i t roa min e (REILLY and HICKIN-CloH1204Se2 Selenium a c e t y l a c e t o n e (MORGAN and DREW) 1456. C,,H,,O,N Substance from the action of ammonia on tetryl (JAMES JONES, C,,H,,O,N B‘-A m i n o-8-p h en ylisobu t y r i c a c i d (SIMONSEN) 569.C,,H,,O,N N i t r o-p-sec. -b u t y 1 p h e n o 1 (REILLY and HICKIXBOTTOM) 123. ~,,H,,ON B e nz y l d i m e t h y l c a r b amid e (WERNER) 1051. P h e ny l-see.-b u t y 1 n i t r o s oa m i n e (REILLY and HICKINBOTTOM) 121, 3 - Cyan o - 2:6 - d i k e t o - 4 -pro p y l p i p e r i d i n e - 5 - c a r b o x y 1 a m id e (‘DAY and THORPE) 1472. l-hiethyl-2-quinolone preparation of (MILLS and WISHART) 585. 2-p-Arninophenyl-Ei-methy1-4-glyoxalon e and its hydrochloride (FARGIIER) 679. BOTTOM) 135. and LEWIS) 1275. Nitro-rt-butylbenzcncs (REILLY and HICKINBOTTOM) 116. 167 FORMULA INDEX. 10 111-11 I1 C,,H,,02N2 N i t r o amino-7t-b u t y 1 benzenes and their salts (REILLY and CloHla02N ad-D i c y a n o-B-p r o p y l g l u t aram i d e (DAY and THORPE) 1471.HICKINBOTTOM) 115. 6-1 mi no-3-c y a n 0-54 a r bam y l-4-pr OF y l-2-p i p c r ido n e (DAY and THORPE), 1472. C,,H,,N,S C1,HlsO,N D i u e t h y l a m m o n i u m benzylcarhamate (WERNER) 1051. Cl0H,,O3N2 d - c a r e n e n i t r o s a t e (SIMONSEN) 574. C,,H,,NI P h en y 1 dime t h y l e t h y lam m oni um iodide mercuri-iodide of and its crystallography (BARKER and PORTER) 1316. C,,HlsN2S (WERNER), 1051. C,,H,,IAS P h e n y l m e t h y l e t h y l a r s i n e niethiodide (BURROWS and TURNER) 1381. C,,H,,12As2 S u b s t a n c e from phenyldimethylarsine and ethyldi-iodoarsine (BURROWS and TURNER) 1379. Substance from phenylmethy!ethylarsine and methyldi-jodoarsine (BURROWS and TURNER) 1381.C,,H,,N,I d2-P h e n y 1 in e t li y 1 pro p y I a z o n i u m i o d i d e ( SINGH) 1211. C,,H,,O,S M e t h y l 7-t h i o d i bu t y r a t e (DAVIES) 304. C,,H,,O,N T r i a c e t y l derivative of d i e t h y l e r i e t r i a m i n e (FARGIIER) 1354. C,,H,,NI Me thyltri-a-propylarnmonium iodide mercuri-iodide of and its B en z y Id i m e t h y 1 t h i o ca r b amide (WERNER) 1051. Dime t h y l am m o n i urn be n z y 1 d i t h io c a r b am a t e crystallography (BARKER and PORTER) 1315. 10 IV C,,H,ONBr Te t rabrorn oni t r ona p h t h a l e n e s (DHAR) 997. C,,H,O,N,S C,,H,,ON,Br 2-Me t 11 yl-4-(2’-a m i n o-5’-br om o p h enyl)-5-gl y ox a1 on e ( + H20), CloHloO,NBr Ace t y 1 derivative of 5-br o m o-o-m e t h o x y b e n z a1 d o xim e (WENT-C a r b op h e’n ox y is0 t h i o h y d a n t o i n ( DIXON and KENNEDY) 79.and its salts (FARGHER) 677. WORTH and BRADY) 1044. 10 v C,,,H1,02N2Cl,S T h i o c a r b a m i d e be n zy 1 t r i c h l o r o a c e t a t e (TAYLOR) 10. CloHl2O2N2Cl2S T h i o c a r bam i d e be n z y 1 d i c h 1 o r oac e t a t e (TAYLOR) 10. C1 Group. CllHloO, C,,H,,N, C,H,,O 3:4:5-Trimethoxyph t h a l i c acid preparation of (ALIMCIIANDAXI C,H,,O E t h y 1 I-a-h y d rox y-8-p h e n y 1 prop i o n a t e hydrolysis of (MCKENZIE C,,H,,O B-Phenyl-a-methoxymethylpropionic acid and its silver salt CllH1602 H om o camphor q u i n o n e (LAPWORTH and ROYLE) 749. CI,H,,03 cyclo H e p t a n e-1:l-diac e t i c a n h y d r i d e (DAY KON and STEVENSON), 645. C,,H,,O a-Ketohomocamphoric acid and its salts (CHORLRY and LAP-WORTH) 739.C1,Hl7N Amino-n-butyltoluenes (REILLY and HICI~INBOTTOM) 133. 4-H y d r oxy-3:5-d im e t h ox y p h t h a 1 i de-2-carb o x y l i c PC i d ( + H,O), &Be nz y 1 i d e n earn i n o-5-ni e t h y 1 g l y o x a l i n e (FARGHER) 676. and its calcium salt (ALIMCHANDANI and MELDRUM) 968. and MELDRUM) 969. and WREN) 689. (SIMONSEN) 567. 4-Me t h y 1 am i n o-n-bu t y 1 benze n e (REILLY and HICKINBOTTOM) 131. Methyl-n-bu t y l a n i l i n e and its salts (REILLY and HICKINBOTTOM) 130, CllHleO Homocamphor (LAPWORTH and ROYLE) 743. 16’1 11 11-11 IV FORMULA INDEX. C,,H,,O cycZoHeptane-1:l-diace t i c acid and its silver salt (DAY RON. and STEVENSON) 639. Homocamphoric a c i d (LAPWORTH and ROYLE) 750.C,,Ha20s CIIHsOeN Tr i xi i t ro-B-n ap h t h oi c acid (DHAR) 1004. C,,H,O,N Cinchonic a c i d methylbetaine (MILLS and WISHART) 586. C,,H,O,Cl 4-H y d r o xy-3:5-di m e t h oxy-2-t r i clil or om e t h y I p h t h a l i d e (ALIMCHANDANI and MELDRUM) 968. C,,H,,0eN4 D i n i t r o-n-b u t y 1 p h e 11 y 1-4-m e t h y l n i t roam i n e ( REILLY and HICKIN BOTTOM) 132. C,,H~,ON (FORYTER and SAVILLE), 156. C,,H,,O,N 1%-Butyl phenylcnrbamate (CHATTAWAY and SAERENS) 710. Cl1Hl5O4Br CllHlsONa T e t r a ni e t h y 1 y-m e t h y 1 f r u c t 0 s i d e (IRVINE and STEELE) 1486. li I11 Camphor q u i n on e c y a n o h y d r azo n e Lac t on o of e t h y 1 a-b ro m o-a-h y d r ox y cyclop en t a n e-1:l-di -4-n- B u t y 1 p hen y 1 me tli y l n i t r 0 s o amin e ( REILLY and HICKIN-C,,H,,O,N l m i d e of cycloheptane-1:l-diacetic a c i d (DAY KON and C,,H170,N a-Camphidonecarboxylic acid and its silver salt (CHORLEY and LAPWORTH) 741.C,,Hl7O,N Acid and its isomeride frGm nitrons acid and camphoroxalic acid (CHORLEY and LAPWORTH) 729. C,,H,,O,Br E t 11 y 1 h y d r o g e n a-b r o m ocyclo p e n t a n c-1:l-dia c e t i c a c i cl (UEUKER and THORPE) 1556. C,,H2,0,N a-isoN i t r o s o h o m o c a m p h o r i c acid (CHORLEY and LAPWORTH), I 40. CllHl,N,Cl dZ-Pli e n y l e t h y 1 a1 1 y 1 a zo nium c h l o ride platinichloride of ( ~ I N G H ) 1212. C,,H,,N,I d l - P h e n y l e t h y l a l l y l s zonium i o d i d e (SINGH) 1212. C,,H,,NI P h e 11 y l d i m e t h y l-a-p r o p y 1 am m o n i urn iodide mercuri-iodide of, P he n y lme t h y 1 d i e t 11 y lam m on ium iodide mercuri-iodide of and its CllH1812As2 Subs t a n c e from pheuylcliethylarsine and methyldi-iodoarsine C,,H,,ON Homo c am p horo x i me (LAPWORTH and ROYLE) 748.CllH26NI E t h y 1 t r i-a-pro p y 1 ammo n i u m iod id e mercuri-iodide of and its a c e t a t e (BECKER and THORPE) 1585. DOTTOM) 132. p-N i t rosom e t hyl-n-bu t y l a n i l i n e (REJLLY and HICHIPI’BOTTOM) 131. STEVENSON) 645. iso N i t r oso h onlo cam pli or ( LAPWORTH and ROYLE) 749. and its crystallography (EAHKER and PORTEE) 1317. crystallography (BARKER and PORTER) 1317. (BURROWS and TURNER) 1380. crystallography (BARKER and PORTER) 1315. 11 IV. C,,H,O,NBr Di ace t y 1 derivatives of d i b r om o h y d r o x y be n ztt 1 d ox im e g (WEXTWOETH arid BBADY) 1042.C1,H,O2NI Cinclionic a c i d methiodide (MILLS and WISHART) 586. C,lHl,0,N2S P 11 e n y l c a r b o me t h o x y is0 t h i o h y d a n t o i n (DIXON and KEN-Cl,H,,O,NCl n-Butyl 2:4:6-tr~chlorophenylcarbamate (CHATTAWAY and SAERENS) 710. Cl,H,,04NBr Ace t y 1 derivotivw of 5-b ro m 0-3 4-d i m e t h ox y b e n z a l d ox i m es (WENTWORTH and BEADY) 1044. CIlH130zNCl n-B u t y 1 2:4-d ic h l or o p h e n y l c a r bam a t e (CHATTAWAP and SEDY) 77. SAERENX) 710, 16’7 FORMULA INDEX. I1 IV-I2 I11 CllHl,0,NBr2 n-B u t y 1 2:4-d i b r o m o ph en y l c a r b a m a t e (CHATTAWAY and SAERENS) 710. Cl1Hl,O2NC1 n-B u t y 1 c h l or 01) hen y l c arba m a t e s (CEIATTARAY and SAEREKS) 710. CllHllOzNBr 96-I3 11 t y 1 b ro ni o p h en y l ca rba ni a t e s (CHATTAWAY and SAERENS), $10.CllH240,NI n - B u t y l p-iodophenylcarbamate (CIIATTAU-AY and SAERENS), I l l . C11Hl,0,N1S2 Cl1H1,O,NC1Br n-B 11 t y 1 2-c h lo r 0.4-bro m o ph e n y 1 c a r bam a t e (CHATTAWAY Ben z y 1-+t h i o u r e a is0 t h i o h y (1 a n t o a t e (TAYLOR) 9. 11 IV and SAERENS) 710. CI2 Group. C,,H,,O 2-H y cl r o x y d i p h e D y 1 a c e t i c .acid (GREENWOOD and NIERENSTEIN), 1598. CI2H,,N B en z i d i n c condensation of benzil with (FERRISS and TURNER) 1143. C1,Hl3As a-Naph t !i y l d ime t h y l a r s i n e (BURROWS and TURNER) 1381. C,,H140 l-PhanylcycZohexan-~-one (BOYD CLIFFORD and PROBERT) 1389. CI,H,,O B en z y l m c t h o x y me t h y 1 m alo n i c acid and its salts (SIMONSEN), 565.C12Hl,0 Lac t o n e of h y d r o x yc a r b e t h o xy m e t h a n e-111:s-3-m e t hpl cyclo-pro p n n e-l-c a r b e t h ox y-2-13 a r b o x y 1 i c a c i d (BEESLEY and THORPE) 616. C,,H,,Br 3-Br o m o-l-p hen y ley& h ex a n e (BOYD CLIFFORD and PROBERT), 1385. C12H160 l-Phcnylc~cZolicxnn-3-o1 preparation of (BOYD CLIFFORD and PEOBEET) 13%. C1,Hl,O Camphoroxalic acid action of nitrous acid on (CHORLEY and LAPWOI~TII) 728. C12HlqN ClzH,,04 C1,H,,Oll 4-Ethylamino-?z-bu! ylbcnzene (REILLY and HICKINBOTTOJI) 132. e t h y l - n - b u t y l a n i l i n e and its picrate (RRILLY and HICKIXBOTTOM) 132. D i e t h y l & p r o p y l g l i i t a r a t e (DAY and THORPE) 1472. Sn c r o s e structure of ( HAWORTH) 199 ; (ARMSTRONG and HILDITCII), 1086 ; mechallisin of the inversion of (JOXES and LEWIS) 1120.12 I11 C,,H,O,N, C,,H,O,N Cl,H,02N, 1348. Cl,H,ON, CI2H,O,N A c en a p h t h en e-2:3-isoox a d i a z 01 e o r i de 8 (ROWE and DAVIES), 1346. C12HB02C1 8 - X a p h t h y l chloroacetate (CROMPTON and VAXDERSTICHELE), 692. C1,HloO,N A cenap h t h ene-2:3-quin onedio xime (ROWE and DAVIES) 1347. Cl,H,,CIAs D i p h e n y l a r s en i o u s chloride (MORGAN and VINING) 777. Cl2Hl,BrAs D i p h en y 1 arsenious bromide preparation of (POPE and Cl2HlOIAs Diphenylarsenious i o d i d e (POPE and TURX’ER) 1452. C12Hl10C1 5-Chloro-l-p henyl-A4-cycZohexen-3-one (BOYD CLIFFORD and C12Hl,0,Br 4-B r om opb en y l d i h y d r o r e s o r ci n (BOYD CLIFFORD and PRO, 3:4-D i n i t roac e n a ph t h en eq u i n one (ROWE and DAVIES) 1350.3-Ni t roacenaph t hen e q u i n one (ROWE and DAVIES) 1349. Ace D a p h t h e n e-7:8-iso o x ad iaz 01 e ox i d e ( ROWE and DAVIES), Acen a p h t h en e-2:3-isooxad iazole (ROWE and DAVIER) 1348. ‘YURX’ER) 1451. P’HOEERT) 1386. BEET) 1385. 167 12 111-13 I11 FORMULA INDEX. C,,H,,ON D i h y d r o a c e t o-a-n a p h t h a1 i d e s (ROWE and LEVIN) 1576. C,,H,,ON Oxime of l-phenylcyctohexan-3-one (BOYD CLIFFORD and C,,H,,O,N 3-Ni t r o-4-ac e t y l amino-n-b u t y l be n zen e (REIT~LY and KICKIN-C12H,,0N Acetylamino-n- and -see.-butylbenzenes (REILLP and HICRIN-C,,H,,ON3 cam p h or q u i n one cy a n oh y d r a z o n e C,,H,,O,N n-B u t y l t o l y 1 car b a m a t e s (CHATTAWAY and SAEREXS) 711. C1,H1,ON B en z y l d i e t h y l c a r b a m i cl e (WERNER) 1051.a n i l i n e and its zincichloride (REILLY and HICKIPSBOTTOM) 132. PROBERT) 1389. BOTTOM) 117. BOTTOM) 111. M e t h y 1 (FORSTER and SAVILLE) 756. derivative of 4-n-Bu t y I phenpl’e t h y l n i t r 0 s o am i n e aiid p-N i t ro s o e t h yl-ir-b u t yl-C1,H,,N,S C1,H,,O,N B a s e from cam1~horqninonecyanoh ydrazone and sulphuric acid (FoRsTER and C,,H1,O,N M e t h y 1 derivative of a c i d CllH1,04N ( CHORLEY and LAPWORTH), C1,H,,O,N D i e t h y l a m m o n i u m be n z y 1 c a r ba m a t c (WERNER) 1051. C12H,,NI P h e n y 1 t ri e t h y l a mni on i uni iodide mercnri-iodides of and their Cl2H2,N,Sz D i e t h y lam m on i u m be n z y 1 d i t h i o ca r ham a t e (WERNER) 1052. C12H,,0N I€ o m o c am p h o r s em i c a r b az one ( LAPWOXTH and ROYLE) 748.C,,H2,0,S E t h y l y - t h i o d i b u t y r a t e (DAVIES) 302. C,,H2,NI T e t r a-a-1) r o p y 1 a m m on i u m iodide mercuri-iodide of and its 12 IV C12H100N3B C12H120NC1 Ox i me of 5-c hloro-l-p h e n yl-A4-cycZo h exen-3-on e (BOYD, C,,Hl2ON,B B or o-a-ph e n yl-P-amin op h en y l h y d r azid e (CHAUDHURI), Be nz y Id i e t h y 1 t h i o c a r b am i d e (WERNER) 1052. (FORSTER and SAVILLE) 758. SAVILLE) 760. 738. Camphor q u i n 0 n em e t h y 1s em i c a r b a z o n e ( + &H,O) crystallography (BARKER and PORTER) 1318. crystallography (BARKER and PORTER) 1316. B or y Id i a z o an) i n o b e n z en e (CHAUDHURI) 1084. CLIFFORD and PROBERT) 1336. lu85. C12H,,0,N2As2 chloride (saharsan) preparation of (FARGHER and PY’MAN) 370.C,2H,,0,N,S 76. B o r y l h y d r a zo am i n o b en z e n e (CHAUDHURI) 1085. 3:3’-Dianiino-4:4’-d i h y d r o xya rsen o benzen e &hydro-P h e n y 1 car b e t h o x y is0 t h i o h y d a n t oin ( DIXON and KENNEDY), C, Group. C1,H,O2 X a n t h o n e formatioii structure and derivatives of (DHAR) 1053. C,,H,N 4-Cyanodiph enyl preparation of (FERRISS and TURNER) 1148. C,,H,,O 2:4-Di h y d r o x y b en z o p h on o n e preparation of (STEPHEN) 1529. C,,H,,O 2:4:4’-Trihydroxyb enzophenone preparation of (STEPHEN) 1529. C,,H120 Substance from the resin of Xanthorrhm (RENNIE COOKE and FIN. C,,H,,As D i p h e n y 1 met h y 1 a r s i n e (BURROWS and TURNER) 1381. C13H14N2 D iam i no d i p hen y l m e t hane preparation of (KING) 988.C130aBrs 0 c t a b r o m o xan t h o n e (DHAIL) 999. 13 I11 C,,H,O,Br H e x a b r om oxan t h o n e (DHAR) 999. Ct,H40aBr4 Tetrabromoxanthone (DHAR) 999. LAYSOX) 347. 16’7 FORMULA INDEX. 13 111-13 IV Cl,H4010N T e t r a n i t r ox a n t 11 one s ( DHAR) 1065. Cl,HsOaN T r i n i t r o x a n t h o ne s (DIIAR) 1064. C,,H60,C1 D i c 11 1 o r o x a n t h o n e ( DHAR) 1069. Cl,HsOsNz D i n i t r o x a n t h o ne s (DHAR) 1063. C,,H70,C1 C l i l o r o x a ~ i t h o i i e s (DIIAI~) 1 O G i . C,,H,O,Br B r o m oxa n t h o n e s (DRAR) 1069. C,,H,O,N C,,H70sN D i n i t r o m o n o a ni i n o x a n t h o n e (DHAX) 1064. C13H,06N D i n i t rox a n t h h y d r o 1 s (DIME) 1067. C13H1006N4 2:4:6-Trinitrophenylbeiizylamine (JAMES JOXES and LEWIS), C,,H,,NAs D i p h e n y l a r s e n i o u s c y a n i d e (MOEGAN and VISIKG) 777.C,,H,,O,N Azo-colourin g ma. t t e r from 3:5-dinitro-o-toluidine and rcsorcinol C,,HllO6C1 4-A ce t oxy-3:5-dim e t 11 ox y-2-t r icli 1 o r om e t 11 y l p h tli a l i d e C,,Hl,0N4 C,,H,,0,N4 3’:4-D i n i t r 0-2:4’-d i a m i n o d i p h e n y 1 m e t h a n e ( KIXG) 990. C,,H,,O,N S u b s t a n c e from aniline and tetryl (JAMES JONES and LEWIS), C,,H,,O,N 4-N i t r o-2:4‘-d i a m i n o d i p h e n y 1 m e t h a n e and its dihydrociiloride C13H1308N7 S 11 b s t a n c e from nt-phenylencdiamine and tetryl (JAMES .JONES and Cl,H,,0,N3 w-I mid e of aa,-d i c y a n,ocycZo h e p t a n e-1 :l-d i a c c t i c a c i d (DAY, C,,H,,IAs a-N a pli t h y l d i n i e t h y l a r s i n e m e t h i o d i d e (BURROWS and TURN-C,,H,,I2AS S u b s t a n c e from a-naphthyldimethylarsine and niethyldi-iodaarsinc C,,H,,ON S em i c a r b a z o n e of 1-p h e n y l cyclo 11 e x a 11-3-0 n e (BOYD CLIFFOED, C1,H1,02N A c e t y l derivative of camphorquinonecyanohydrazono C,,H190W Ace t ylaniino-n-bu t y 1 t o l uene s (REILLY and HICKINBOTTOM) 133.C,,H,,O,N 0-1 mid e of aq-di c a r bam y lcyclohe p t ane-1:l-diac e t i c a c i d C1,H2,0,Br E t h y l a d - d i b r om ocyclopen t a n e-1:l-d i a c e t a t e ( BECKER and C,,H,,O,N3 Base from camphorquinonecyanoliydrazone and hydrochloric acid C,,H,,O,N Dim e t h y l derivative of a c i d Cl1H,,O,N (CHORLEP and Larwowir), C,,H??O,Br E t h y 1 a d - b r om ocyclop e n t a n e-1:l-d i a c e t a t e (BECKER atd C,,H2,NI P h e n y l d i e t 11 yl-a-p r o p yl a m m o n i urn i o d i d e mcrcuri-iodide of, N i t r ox a n t h o n e s (DIIAR) 1061.1275. D i p h e n y 1 c y a n o a r s i 11 e (MCKENZIE and ~~TooII) 411. (MORGAN and DREW) 791. (ALIMCHANDANI and hIELDItUM) 365. ide (KING) 992. 4:4‘-D i a m i no-2:2’-a zo x y d i p h e n y 1 m e t h a n e and its dihydroclilor-1275. (KING) 989. LEWIS) 1278. KON and STEVEXSOS) 648. ER) 1381. (HURROWS and TURNER) 1382. and PKOBERT) 1389. (FORSTER and SAVILLE) 75i. (DAY KON and STEVEXSON) 644. THORPE) 1585. (FORSTER and SAVILLE) 757. 788. 1 HORPE) 1586. and its crystallography (B.~RKEK and PORTER) 1319. 13 IV C13H,01,N4C1 C h l o r o t e t r a n i t r o x a n t h o n e s (DIIAR) 1068.Cl3H,Ol0N,Br B r om o t e t r a n i t r o x a n t h on es (DHAR) 1070. C,,H,0sN2C1 D i c h l o r o d i n i t r ox a n t ho n e (DHAR) 1069. CSsH4O&Bra D i brom o d i n i t r ox a n t h o n e (DEAR) 998, 167 13 IV-14 111 FORMULA INDEX. C13H40,N3C1 C h 1 o r o t r i n i t r o x a n t h o n e ( DIIAR) 1 068. C13H,0,N2C1 C h l or o d i n i t r o x a n t h one (DHAR) 1069. C,,H,O,N,Br R r om o (1 i n i t r oxan t h on e (DHAR) 1070. C,,H,O,CI,Sn Substance from stannic chloride and 2:3:8-trihydroxyxanthone Cl,H,O,N2C1 4:4’-Di c h 1 or o-3:3’-d i n i t r o d i p hen y lm e t h a n e (STEPHEN, Cl,H,,02NB B en z oy 1 b o r a n i 1 id e (CHATJDHURI) 1082. C13HloNC12A~ D i p h e n y l c y a n o a r s i n e d i c h 1 o r i d e (MCKENZIE and WOOD), 416. C13H110NSA~2 3’-A ni i n o -4'-h y d ro x y-l:3-d i a z o 1 e-5:l’-ar s e n o b e n ze n e and its hydrochloride ( PARUHER) 876.C13H140N3C1 S emi c a r b azo n e of 5-c h 1 oro-l-ph en’yl-A4-cycZo h ex e n-3-0 11 e (BOYD CLIFFORD and PRORERT) 1386. 13 V (DEAN and NIERENSTEIN) 805. SHORT and GLADDING) 523. C,,H,O,NBrB Ben is o y 1-p-b r o m o b o r a n i 1 i d e (CHAUDHURI) 1084. CI4 Group. C,,H,N 4:4’-Dicysnodiphenyl preparation of (FERRISS and TURNER) 1149. C,4Hlo02 B enzil condensation of benzidine with (FERRTSS and TURNER) 1143. C,4Hl,0s 2:3-Dihydroxy-8-methoxyxanthone preparation of (DEAN and C,,H,,O 4-Phenylacetophenone preparation of (FEREISS and TURNER) 1147. Cl4HlE0 Ace t y l derivative of l-phenylc~cZohexan-3-ol (BOYD CLIFFORD and C14H,,06 E t h y l ni e t h y 1 m e t h a n e-III1’”%ycZop r o pan e-l:2:3-t r i c a r b ox y 1 a t e C1,H,206 B o r n y l hydrogen t a r t r a t e s and their salts (WEEN W I L L I A m , Cl,H,,N 4-Am i n o-l:3-di-n-bu t y l b enz en e (REILLY and HICKINBOTTOM) 123.C,,H,,O D i m e t h y l h y d r o c a m p h o r y l a c e t a t e (LAPWORTH and ROYLE) 747. C,,H,O,Br 1:3-D i b r om o a n t h ra qu i none ( DHAR) 1002. C,,H,O,N 1:3-D i n i t roa n t h r a q u i none (DHAR) 1003. C,,H,O,N 3-Ni t r o-l-a m i noa n t h r a q u i n o n e (DHAR) 1003. Cl,H,,0,N4 D i n i t r o a z o t o l u e n e (KENNER and PARKIN) 857. Cl~Hl106NP 2:4:6-Tri n i t r o p h e n yl-m-x y 1 y lain i n e (JAMES JONES and C,H,,O,N P h 1 or oa c e t op h e n o n e p h e n y 1 h y d ra 80 n e (SEN and GHOSH) 63. C14H,,0,As2 Cl4Hl4O8N6 S u b s t a n c e from niethylaniline and tetryl (Janms Joms and Substance from 0 and p-toluidines and tetryl (JAMES JOKES and LEWIS), ClpHl,06As a c i d C14HleC1,AS S 11 b s t a n c e from phenyldimethylarsine and phenyldichloroarsine Cl4H1,I,As S u b s t a n c e from phenyldimethylarsine and phenyldi-iodoarsine Cl,Hl,O,N CS4H&BP NIERENSTEIK) 803.R ROBERT) 1388. (BEESLEY and THORPE) 617. and MYDDLErox) 194. 14 I11 LEWIS) 1277. D i h y d r ox y d i m e t h o x y a r s e n o b e n z e n e s (FARGHER) 872. LEWIS) 1278. 1276. (PARGHER) 873. (BURROWS and TURNER) 1379. (BURROWS and TURNER) 1379. E t h y 1 4:4’-D i h y d r o s y-3:3’-d i m e t h o x y d i p h e n y 1 a r s i n i c 8-Pr op y l g 1 u t a ri c s e m i a n i l i de (DAY and THORPE) 1472.b r o m o c a r b e t h o xy m e t h a n e-IP3-3-m e t h ylcyclo. prop a n eVl:2-dic a r b o x y l a t es (BEESLEY and THORPE) 615, 167 FORMULA INDEX. 14 III-i6 I11 C14Hz106Br3 E t h y l aB&t r i b r om o dime t h y l p r opan e t r icarb o x y 1 a t e (BEEB-C14H,,0N 4-n-B u t y l p h e n y l-n-b u t y 1 n i t r o s o a m i n e (REILLY and HICPIN-C,,H,,O,Br E t h y 1 BB-di b r o m o d i m e t h y 1 p r o p a n e t r ica r b o x y l a t e (BEES-LEY and THORPE) 619. BOTTOM) 124. LEY and THORPE) 610. 14 IV C1,H,O2N2Br C14H1204N,S D i n i t r o d i t o l y l s u l p h i d e (KENNER and PARKIN) 857. CldHlaOsNzAsa Cl,Hl,O,N,S Methyl-orange effect of temperature on the colour changes of ClPHl6O,N2As D jam i n o d i h y d r ox y dim e t h oxy a r s en o b en z e n e s and their a- and 8-P h t h a1 y l-p-b r o m op h en y 1 h y d razid e s (CHATTAWAY and TESH) 715.5:5'-D i n i t ro (1 i h y d r o x y d i m e t h ox y a rsen o b e n z en es (FARGHEK) 873. (TIZARD and WHISTON) 150. hydrochlorides ( FARGHER) 87 3. CI5 Group. ClSHZ4 d-Longifolene and its salts (SIMONSEN) 578. C15Hs05 8-Hydroxy-2:3-quinoxanthone preparation of (DEAN and NIEREN-Cl6H8O4 A n t h r a q u i n on e-l-c a r b oxy l i c a c i d preparation of (PERKIX) 706. C15Hlo0 2:3-Me t h y l e n e dio xy-8-m e t h o x y xa n t h one preparation of (DEAN C,,H,,O 3-P h e n y 1 d i h y d r o c o u ma r i n preparation of (GREENWOOD and C16H1206 8-Hydroxy-2:3-ctime t h o x y x a n t hone (DEAN and NIERENSTEIN), 806.Cl6HI2Oe Colouring m a t t e r (+ 2H20) from Hyeizanche globosa (HENRY) 1625. CI5Hl40 3-Phenylchroman (GREENWOOD and NIERENSTEIN) 1597. C15H1,0 Catechin constitution of (NIERENSTEIN) 971 1151. Cl5Hl60 2-H y dr oxy-aa- and -a?-dip h en y l p r opan es (GREENWOOD and C16H16Oa 2:o-D i h y d r o x y-aa-d i p h e n y 1 propane (GREENWOOD and NIEREW-C15H17As Di-o-tolylmethylarsine (BURROWS and TURNER) 1383. C15H1& n- and iso-Hiyenanchin (HENRY) 1619. 15 111 C15H,0,N 5:5'-D i n i t r ob e n z o p h en o n e-2:2'-d i c a r b o x y l i c a c i d (STEPHES, SHORT and GLADDING) 527. Cl5HlOO,N a-Ph t h a 1 y 1 form y l p h e n y l h y d r a z i d e (CHATTAWAY and TESH), 717. Cl5H,,OZN2 a- and B - P h t h a l y l t o l y l h y d r a z i d e s (CHATTAWAY and TESH) 716.C15H1303N3 p-Ni t r op h en y 111 y d raz o n e s of m e t h y 1 c o um a r a n o n e s (HIGGIN-C15H150N 4-A c e t y l a m i n od i p h e n y 1 m e t h a n e (KING) 990. Cl,H150,N Tolyloxyacet a n i l i d e s (HIGGINBOTHAM and STEPHEN) 1540. C15H~,06N3 w-Me t h o x y r e s a c e t o p h e n o n e p-n i t r o p h e n y 1 h y d r a z o n e Cl5H1,O3N A n i l i c a c i d of cis-qclo p e n t a n e sp'~ocycZop r op a n e-l:2-d i c a r b-15 I1 STEIN) 802. and NIERENSTEIN) 803. NIEREXSTEIN) 1596. NIEKENSTEIK) 1595. STEIN) 1596. BOTHAM and STEPREN) 1541. (SLATER and STEPHEN) 313. oxylic acid (EECPER and TIIORPE) 1588. 167 15 111-16 IV FORMULA INDEX. C15H,,NI P h e n y 1 be n z y 1 dime t h y 1 am in o n i u m i o d i d e mercuri-iodide of, C1,H,,IAs P h e n y 1 d i m e t h y 1 a r s i n e b e n z i o d i d e ( BURROWS and TURXER), CI5Hl8I2As2 S u b s t ance from pheiiylmcthylethylnrsine and phenyldi-iodoarsine and its crystallography (BARKER and PORTER) 1319.1378. (BURROWS and TURXER) 1381. 15 IV C,,H,O,N,Br a-P h t h a 1 y 1 form y l-p-b r o in o p h e n y 1 h y d r a z i d e C,,H,,O,Cl,Sn (CHATTAWBY Substance from stannic chloride and 5-hydroxy-2:Y-dimethoxy-and TESH) 717. . xanthone (DEAN and NIERENSTEIN) 805. C16 Group. C16H1206 5:7:2’:4’:6’-Pe n t a h y d r o xy-2-1) h e nyl-4me t hylene-l:4-benzopyr a n CI6H15O2 4:4’-Diacetyldiphenyl and its condensations with aromatic arnincs C16H180 2-H y ti r o xy-aa- and -ay-d i p 11 e n y 1 p r o p a n e m e t h y 1 e t h e r s (GREES-C,,H,,N C a m p h a n o d i h y d r o q u i n o x a l i n e (B.K. and D. SINGH DUTT and CleH,05 E t h y 1 ben zy lme t h o x y m e t h y 1 ma 1 on a t e (SIMONSEN) 566. Cl6H3,OI1 Anhydro-acid from t e t r a m e t h y l f r u c t o s e (HAWORTH) 208. Cl6H8O,N2 ci6H,203N2 (SEN and GHOSH) 62, (FERRISS and TURNER) 1140. WOOD and NIERENSTEIN) 1595. G. MINGH) 986. 16 111 N i t r o x a n t h o q u i n o 1 i n e (DHAR) 1066. a- and B-P h t h a 1 y 1 a c e t y l p h e n y 1 h y d r a z i d e s (CHATTAWAY and a-P h t h a1 y 1 form y 1 t o 1 y 1 h y clra zi d e s (CHATTAWAY and TESH) 718. TESH) 717. C1,H,,0,N3 2:4-D i n i t r o p h en y 1 d i €I y d r o - a - n a p h t h y l a m i n e s ( ROWE and C16Hl,0zN2 a- and B-P h t h a1 y 1 p h e n y 1 e t h y l 11 y d r azi d c s ( CHATTAWAY and Cl~H180zN4 E t h ylid en eb i s phen y l c a r bam ide (FARGHER) 679.ClsH1803N2 2:2’-Di m e t h oxy-3-3’-az oxy t oluen e ( KENNER and PARRIN) 856. C16H180,AS 3:4:3’:4’-T e t r a m e t h o x y a r s e n o b e n z e n e (FARGHER) 870. C,,H,,O,N isoNi t r o s o cam p h o r N-ph e n y l e t h e r (FORSTER and SAVILLE), 761. C16Hl,N21 dl-Ph en y l be n z y l a l l ylazon i u m iodide (SISGH) 1212. Cl6HzoONz P h e n y l b e n z y l a l i y l a z o n i u m h y d r o x i d e salts of and their resolution (SINGH) 1213. C,,H2,NI P h e n y 1 be n z y 1m e t h y l e t h y 1 am in o n i u in iodide mercuri-iodide of, and its crystallography (BARKER and PORTER) 1320. C16H2,1AS Di-o-t o l y 1 m e t h y I a r s i n e me t h i o d i d e (BURROWS and TURNER), 1383. CI6H2,N2C1 Ph e n y 1 b enz y 1 p r o p y 1 az o n i u tn c h 1 o r i d e aud its salts (SINGH), 1207.Cl~H21N21 P h en y l b e n z y I p r o p y l a z o n i u tn i o d i d e (SINGH) 1207. C16H220N2. Phenylbenzylpropylazonium h y d r o x i d e salts of and their 16 IV C,,H,O,N,Br a-P h t h a1 y 1 a c c t y 1-p-b r om o p hen y l h y d r a z id e LEVIN) 15’17. TESH) 712. resolution (SINGH) 1208. (CHATTAWAY and TESII) 717. 167 FORMULA INDEX. 16 IV-I7 I11 C,~H~,ONBI? C,,&OO,N~AS, Bromophenylaininocamphor optical rotation of (B. K. and D. SINGII DUTT and G. SINGH) 983. S u b s t a n c e from reduction of 5-amino-3:4-dimethoxyphenyl-arsinic acid (FARGHER) 872. CI7 Group. C,,H,O, C,,H,,O C17Hlo02 H y d r o x y b e n z a n t h r o n e and its snlphate (PERKIN) 698.C17H,,0 B e n z a l i z a r i n aud its salts (PEEKIN) 702. C,,H,,O 8- Ace t o xy-2:3-cli me t h o x y x a n t 11 one (DEAN and NIEILENSTEIN), 805. C17Hl,N Benzylidenediliydro-a-naphthylamines (ROWE and LEWIS) 1576. C17H1604 E u x a n t h o n e d i e t h y l e t h e r salts of (PERKIN) 699. C17H,,N Beu z y l i d e n e-ar-t e t r a l i y d r o-a-nap h t h y 1 n m i n e (ROWE and LEVIN), 1579. C1,H,,O2 B e n z o y l derivative of p-scc.-butylphenol (REILLY aud HICKIN-BOTTOM) 123. 17 111 K e t o d i 1 a c t o n e of b e n z o p h e n o n e-2:4:2’:4’-t e t T ac a r b o x y li c a c i d , B e n z a n t h r o 11 e properties of and its salts (PERKIN) 696. and its resolution (MILLS and NODDEB) 1407. Cl,H1,05N, C1,H1,,O2N2 IEBH) 714. C,,H1403N2 718.3:5-D i n i t r o t o l u e n e-2-az o-&nap h t h o l (MORGAN and DREW) 791. a- and B-P h t h a 1 y 1 p h e n y 1 a1 1 y 1 h y d r a z i d e s ( CHATTAWAY and a-P h t h a1 y 1 a c e t y 1 t o l y 1 h y d r a z i d e s ( CEIATTAWAY and TESH), a-P h t h a1 y 1 p r o p i o n y 1 p h en y l h y d r a z i d e (CHATTAWAY and TESH) 717. C17H1108N6 S u b s t a n c e from naphtliylamines and tetryl (JAMES JONES and LEWIS) 1277. C,,HI5ON3 2-p-Ben z y l i d e n e a m i n o p h e n y 1-5-m e t hyl-4-gl yoxn 1 one ruid its acetate (FARGHER) 679. CI,H,,O2N2 a- and B-P h t h a 1 y 1 p h e n y l p r o p y 1 h y d r a z i d e s (CHATTAWAY and TEYH) 713. C1,Hl,06N4 4:3’-D i n i t ro-2:4‘-diac e t y 1 a i n i u o d i p h e n y 1 III e t h a n e (KING), 990.C1,H170,N3 D i a c e t y l derivative of 4-ni t r o-2:4’-di a m i n o d i p h e n y l m e t h a n e (KING) 989. C17HI,0N Re n z o y l a m i n o-72-b u t y 1 be n z e n e s (REILLY and HICKINBOTTOM), 111. C,,HI,02N 4-n-I3 u t y l p h e n y I p h e n y 1 c a r b a m a t e (REILLY and HIC‘KIX-BOTTOM) 115. CI,H2,ON2 a-P henyl-B-4-n- and sec. -bu t y l p h e n y l c a r b a m i d e s (REILLY and HICKINBOTTOM) 112 120. C1,H2204N2 P h e n y l h y d r a z o n e (+H,O) of a - k e t o h o n i o c a m p h o r i c a c i d ( CHORLEY and LAPWORTH) 740. C,,H-22NI P h e n y 1 b e n z y 1 d i e t h y l a m m o n ium i o d i d e mercuri-iodide of and its crystallography (BARKER and PORTER) 1320. P h e n y 1 b e n z y l m e t h yl-a-pr o p y l a m ni o n i u m i o d i d e mercuri-iodide of a i d its crystallography (BABKER and PORTER) 1321.C,,H,ON T o l y l a m i n o c a m p h o r optical rotation of (B. K. and D. SINGH, DUTT and G. SINGH) 982. C,,H,02N o-Methoxyphenylaminocamphor (B. I(. and D. SINGH DUTT, and G. SINGH) 985. CI7Hz8O3N cycloHeptsne-l:l-diacetic a c i d s e m i a n i l i d e (DAY KON and STEVENSON) 645. 167 7 III-I9 I1 FORMULA INDEX. C17H8,0N8 S u b s t a n ce from suberone ethyl cyanoacetate and ammonia (DAY, KON and STEVEXSOX) 646. 17 IV Cl7H1,O,N,Br a- and 6-P h t h a1 y I-p-b r om op h en y 1 a1 l y 1 hydra zi d e s (CRATTA-WAY and TESH) 715. C,,H,,O,NzS P h en y Ic ar box y-o-t o 1 y liso t hio h y da n t oin (DIXON and KEN-NEDY) 77. CI8 Group. a C18HlzOz Methoxybenzanthrone and its salts (PERKIN) 698.CIPHIPO 2:3-Diace t oxy-8-me t h ox y x a n t h one preparation of (DEAN and C18H15A~ T r i p h e r y l a r s i n e preparation of (BURROWS and TUI~KER) 1382 ; C18H15Bi Triphenylbisiiinthine molecular weight of and its salts (CIiac-NIEILENSTEIN) 804. (POPE and TURNER) 1447. LENGER and GODDARD) 765. CJI,,O 3:5:3’:4’-T e t ram e t h o xy-2-phe n y lc o urn a r an-l-on e (NIERENSTEIN), 1155. C18H2,07 CI8H,,O2 2’-Hydr O X y-3 4:4’:6’-t e t ra m e t 11 ox 9 d i p h e n y 1 a c e t i c a e i d (NIER-Oleic acid sodium salt investigations of solutions of as curd gel, ENSTEIN) 1154. and sol (LAING and MCBAIN) 1506. 18 I11 CleHI,05N 3:4-D i n i t r oac en a p h t h e n e q u i n on e-7-p h en y I h y d raz one C18Hl103N 3-N i t r oac e n a p h t h e neq u i n on e-7(or 8)-p h e n y 1 h y d r az one C18H1208N2 l-&An t h r a q u i no nyl-3-m e t h y 1-5-p y r a zolo n e ClsH,,O,N 4-B-An t h r a q u i n one azo-3-m c t h yl-5-p y razol one C18H,602N2 a- and B-P h t h a l y l-p-t o 1 y la11 y 1 h y d r a z i d e s (ROWE and DAVIES) 1351.(ROWE and DAVIES) 1350. 1268. 1270. TESH) ’716. (SAUNDERS) , (SAUNDEBS), (CHATTAWAY and CI8Hl6O3Nz a-P h t h a1 y l-n-bu t y r y 1 p h e n y 1 h y clr a z i d e ( CHATTAWAY and TESH) 717. C18H,,02N8 Ben zo y 1 derivative of C18Hz,0,C1 camphor qui n o n ec y an o h y d ra z o n e 3:4:2’:4‘:6’-Pe n t ame t ho x y d i p h en y Ime t h y 1 chl o r i d e ( XIEREN-(FORSTER and SAVILLE) 756. STEIN) 978. 18 IV C,,HI,OsN4B B o r o-a-p h e n y 1 h y d r a z i d o b e nz en e az op h en o 1 and its hydro-chloride (CHAUDHURI) 1085.CI9 Group. ClDHI4O3 Dirnethoxybenzanthrone and its salts (PEI~KIN) 703. ClDH16N2 0-8 m i n ocin nam y l i d e ne q 11 i n a l d i n e and its diliydrochloride ClSH2,O Benzo y l derivative of l-phenylcyclohexan-3-01 (BOYD CLIFFORD, ClSH22O7 3:4:2‘:4’:6’-P e n t a,m e t h ox y d i p h e n y 1 a c e t i c acid and its sodium salt a c i d (NIER-(MILLS and EVANS) 1038. and PROBEET) 1388. (NIERENSTEIN) 977. ENSTEIN) 975. 2:4:6:3’:4’-P e n t am e t h o x y d i p h e n y 1 m e t h a n e-3-ca r bo x y l i c 168 FORMULA INDEX. 19 11-20 I11 C1,H& 2’-H y droxy-3:4:4’:6’-te t r am e t h ox y-aa-d i p h e n y l p r op a n e (NIER-ClrHaeOs Z-Menthyl atrolactinates and their hydrolysis (MCKENZIE and hydrolysis (Mc-ENSTEIN) 1154.WREN) 686. KENZIE and WREN) 690. &Men t h y l d-a-h y d r o xy-B-p h e n y l p r o p io n a t e and its I 9 I11 CleHlSOaN A n i l i n o x a n t h o ne (UHAR) 1068. CloHl,O,N p-N i t r o c i n n a m y 1 i d e ne q u i n a l d i n e (MILLS and EVAKS) 1038. CloHl,08Ns T r i a c e t y l derivative of azo-colouring m a t t e r C1sH1105N3 CleHl,04N3 (SAUNDERS), CI,H,,O,N o-N i t r ob e n z o y 1 derivative of 1 -p h e n y I cyclo h e xan-3-0 1 (BOYD, CleH2106Cl 3:4:2’:4’:6’-P en t aru e t h o x y d i p h e n y l a c e t y 1 c h 1 o r i d e (NIEREN-(MORGAN and DREW) 791. 1272. CLIFFORD and PROBERT) 1388. STEIX) 1153. 4-&An t h r a q u i n o n ea z o-3-m e t h y lisoo xazolone Czo Group; C,H140 P h e n o l p h t h a l e i n preparation of (COPISAROW) 212.C,Hl,O 4-Diphenylyl b e n z y l k e t o n e (FERRISS and TURKER) 1148. Ca,H& 2’-Ace t ox y-3:4:4’:6’-t e t r a me t h ox y d i p hen y l a ce t i c a c i d (NIEB-C,H,O 2:4:6-Trim e t h ox y p h en y l 3:4-dim e t h o xy-8-p h e n y l e t h y l ketone C2,H,07 M e t h y l 3:4:2‘:4’:6’-p e n t a m e t h o x y d i p h e n y 1 ace t a t e (NIEREN-ENSTEIN) 1155. (NIERENSTEIN) 976. STEIN) 978. (NIERENSTEIN) 976. ENSTEIN) 976 1153. Me t 11 y 1 2:4 :6 :3’:4’-p e n t a me t h o x y d i p h e n y 1 m e t h a n e-3-c a r b ox y I a t e C,H2,0a 3:4:2‘:4‘:6’-P e n t a m e t h o xy-aa- and -ay-di p h e n y l p r o p a ne s (NIER-2:4:6:3’:4’-Pen t ame t h o xy-3-e t h y l d i p hen y l m e t h a n e (NIERENSTEIN) 975. CaoH2,#6 2:4:6:3‘:4’-P e n t am e t h o xy-3-e t h y 1 d i p h en y 1 c a r b i n o 1 (NIEREN-C,,,H,,N D i a zoainino-4-1%-bu t y l b e n z e n e (REILLY and HICKINBOTTOM), 20 111 STEIN) 974.113. C2,H,,03N2 Azine from 8-hydroxy-2:3-quinoxanthone and 3:l-tolylenediamine C2,H1,ONa o-F orm y I am i n oci n n am yl i d e n e q u i n a1 d i n e (MILLS and EVANS), C,H160,N E t h y I &ant h r a q u i n o neaz oace t o a c e t a t e (SAUNDERS) 1271. CIOHIs06N6 Substance from m-toluidine and tetryl (JAMES JONES and Ca,H,&,I o- A In i n o c i n n a my li d e n e q u i n a1 d i n e m e t h i o did e (MILLS and CzoHtoON2 4-n-Butylbenzeneszo-8-napht h o l (REILLY and HICKINBOTTOM), C,H,O,N (REILLY C2,H,IAs D i p hen y lm e t h y l a r sine b enz i o d i d e (BURROWS and TURNER), CmH220nN2 4-n-R u t y 1 b enz e n ea z o ben zo y l a c e t one (REILLY and HICKTN-(DEAN and NIERENSTEIN) 803.1038. LEWIS) 1276. EVANS) 1040. 113. and HICKINBOTTOM) 114. 1381. BOTTOM) 114. 4-n-B u t y l b e nze n e azo-2:7-d i h y d r o x y n a p h t h a 1 en e CXVII. 1681 3 20 111-22 111 FORMULA INDEX. C2,H,0N a- and B-Naphthylaminocamphor optical rotation of (B. K. and C,H2s0,C1 3:4:2’:4’:6’-Pe n t a me t h o x y d i p h e ny 1 met h y 1 c h l o ro m e t h y 1 C20H2402N2 Quinine ferrocyanides of (BRIGGS) 1034. C2,,H,,0N ur-T e t r a h y d r o-a-na p h t h y lim i 11 o camp h or preparation and rotation of (B. I(. and D. SINGH DUTT and G. SINGH) 987. C,,H2,0N ar-Tetrahydro-a-naphthylaminocamphor (B. K and D. SINGH, DUTT and G. SINGH) 987.D. SINGH DUTT and G. SINGH) 986. k e t on e (NIERENSTEIN) 1153. 20 v C20H210NaClaCo D i c h 1 o r o t e t r a p yr i d i n e c o b a 1 t h y d r oxi d e salts of (PRICE) 860. Czl Group. CalHlaO D i ace t o x y l~ en zan t h r one (PEBKIN) 701. C2,Hz,As Tri-o-tolylarsine (BURROWS and TURNER) 1382. CzlHaaO Apigenin t r i e t h y l e t h e r salts of (PERKIN) 699. C2,Ha,0 Me thy1 derivative of 2:4:6:3’:4’-p en t am e t 11 oxy-3-e t h yldiph e 11 y 1. carbinol (NIERENSTEIN) 974. 21 111 C,,H,,N,Cl C hl orome t h y 1 b en z op h e nan t hrazi n e s (MORGAN and DREW), 789. C21H,,ON2 o-A ce t y l a m i n ocinna m y 1 ide ne q uinald i n e (MILLS and EVANS), 1039. C2,Hl,02N2 Car box y m e t h y 1 am i n o c i n n am y 1 i d ene quin aldine (MILLS and EVANS) 1039.C2,H2,0,Na Te t ra-ac e t y 1 derivative of 4-ni t ro-2:4’-d iam i n od i p h en yl-methane (KxxG) 990. C~~HaaO~Na Dian i l i d e of trans-cyclo p e n t a n e spirocycclo prop an e-1:2-d i c a r b-oxylic acid (BECKER and THORPE) 1587. C2,H2,0aN2 E t h y 1 4-p-dim e t h y lami nop h e nyl-2:6-dim e t hy 1 p y r i d in e di-carboxylate and its potassium salt (HINKEL and CREMER) 139. CzlHneOdNa E t h y 1 4-p-di m e t h ylam i n o p he nyl.2:g-dim e t h y 1-1:4-d i h y d r o-pyridine-3:5-dicarboxylate and its salts (HINKEL and CREMER) 138. 21 IV C2,Hl,0,N,B~ a-P h t h a 1 y 1 be n z o yl-p-b r o m o p h e n y l h y d r az ide (CHATTA-WAY and TESH) 718. Cza Group. CaoHlclOl 2:7-Dimethylfluoran preparation of (COPISAROW) 215. CasH1804 o-Cresolphthalein preparation of (COPISAROW) 214.CahHS80 Ace t y 1 derivative of 2:4:6:3’:4’-pen t a m e t h oxy-3-e t h y l d i p h e n y 1-c arbino 1 (NIERENSTEIN) 974. 22 I11 CaaHlaOsNs a-P h t h a1 y 1 b en z u y 1 t ol y 1 h y dr az i de s (CHATTAWAY and TESH), 718. C,2H1,BrsBi Dip hen y l-a-na p h t h y 1 b ism u t hin e dibro mide (CHALLENGEE and GODDARD) 772. CBaHzoONz Ben z o y liso p rop y li d en e ben z id ine (FERRIS and TURNER) 1146. Ca,HaJAS Tri-o-t o l y l a r s i n e me t h i o dide (BURROWS and TURNER) 1382. 168 22 IV-27 I1 FORMULA INDEX. 22 IV CraHolONaI Ace t y 1 am i n o c i n n am y 1 i d e n e q u i n a l d i n e m e t h i od i d e (MILLS and EVANS) 1039. Cza Group. CoaHa60s L u t e o l i n t e t r a e t h y l e t h e r salts of (PERKIN) 699.CasH,,O,N D i n i t r o x a n t h on e az o-8-n a p h t h o 1 (DHAR) 1064. 23 I11 CZ4 Group. Ca4HasNo 2:3-Dip h en yl-6-n-bu t y l q u i n ox a li ne (REILLY and HICKINBOT-CaJIzrNo 2:4:8:2’:4’:8’-H exam e t h y 1-6:6’-di q u i n 01 y 1 and its platinichloride Ca,HssOa D i b o r n y l t a r t r a t e s (WREN WILLIAMS and MYDDLETON) 193. CarHs,O Alcohol from Eyenanchc globosa (HENRY) 1624. C,,H,O,N 3-N i t r o a n t h r a q u i n on e-l-az o-8-n a p k t h o 1 (DHAR) 1003. Ca4H1603N4 4-B e n zen e azo-l-&an t h r a q u i n o n yl-3-m e t h yl-5-p y r az o 1 one Cap~a,ON B enzo y 1 iso p r o p y 1 i d en e t o l i d i n e (FERRLSS and TURNER) 1147. C2,HtsOaNa D i ac e t yl isop r o p y 1 i d e n e t o li d i n e (FERRISS and TURNER) 1146. TOM) 118. (FERRIS and TURNER) 1146.24 111 (SAUNDERS) 1268. CZ5 Group. Cz5Ha,03N3 T r i b e n z o y 1 derivative of d i e t h y 1 e n e t r i a m i n e (FAROHER), 1354. Ca6HasNaBP 1:l’-D i e t h y 1 car b o c y a n i n e bromide (MILLS and HAMER) 1558. Ca5Hz5NaI C,I;H,0,$J4Br S ubs t a n c e (+ 2H20) from oxidation of 1:l’-diethylcarbocyanine 1:l’-Dl e t h y 1 c a r b o cyan i n e i o d i d e (MILLS and HAMER) 1557. 25 1V bromide with nitric acid (MILLS and HAMER) 1561. CaS Group. CaeH,On Ace t y l derivative of ‘5:7:2’:4’:6’-pen t a h y d r ox y-2-p henyl-4-CaaH,sNs 4-n-Bu t y1 benze ne azo p h enyl-B-n a p h t h y l a min e ( REILLY and HICK-C,6Hsa02 A c e t y l derivative of alcoh 01 C2rH,o0 (HENRY) 1624. 26 111 CJIa603NS Ace t y lisopr o p y 1 i d e n e t o l i d i ne (FERRISS and TURNER) 1145.Ca6H,,0,N2 m-Phenylenebisaminocamphor (B. K. and D. SINGH DUTT, mcthyleae-l:4-benzopyran (SEN and GHOSH) 62. INBOTTOM) 113. and G. SINGH) 985. Cz Group. Ca7HarO8 Cs,Hz60,No A c e t y 1 is0 pr o p y 1 i d e n e b e n z o y 1 isopr o p y 1 i d en e be n z i d i n e Ca,Hs,01N4 m-Tolylenebisiminocamyhor preparation and rotation of (B. Ii. Ca7HS8OaNs m-Tolylenebisaminocamphor preparation and rotation of (B. K. M y r i c e t i n h e x a e t h y l e t h e r salts of (PERKIN) 699. 27 I11 (PERRISS and TURNER) 1146. and D. SINGH DUTT and G. SINGH) 984. and D. SINOH DUTT and G. SINGH) 985. 168 28 1 1 - 4 4 I1 FORMULA INDEX. C28 Group. Cz8Hz4 CZ8Hl6O3 a- and B-N a p h t h a fl u o ran 8 and a-N a p h t h o l p h t h a l e i n s prepara-C,,H,,O 4:4’-Dip h e n y l d iac e t y l d i p h e n y l (FERRISS and TURNER) 1150.C,,H2,02 D i a c e t y 1 derivative of 9:lO-dip h en yl-9:lO-d i h y d r oa n t h r a c e n e CZ8H4,0 C,,H1,0,N4 Dime t h y l-9:lO-dip hen yJ-9:lO-di h y d r o an t h r a c ene (RAY) 1338. 28 11 tion of (COPISAROW) 216. (RAY) 1337. P h y t o s t e r o l from Hyenanche globosa (HENRY) 1624. 28 111 4-&An t h r a quinon e a z o-l-B-naph t h yl-3-me t h yl-5-pyrazol one (SAUNDERS) 127 1. ones (SAUNDERS) 1269. 4-a-and-B-N aph t h a1 e n e az 0-1 -&ant h r a q u i n onyl-3-ni e t h y 1-6-p y r azol-C, Group. C,,HZ8 C,oH,sOa C,,H2,CI,Bi T ri-a-n a p h t h y 1 bismuth i n e d i c h 1 o r i d e (CHALLENGER and GOD-C,,H,,O,N? 1:4-Naphthylenebisirninocamphor (B. K. and M. SxNGH), D i m e t h y 1-9:lO-di t olyl-9:lO-di h y d r o a n t h r ac en e (RAY) 1338. 30 I1 Acetyl derivativc of p h y t o s t e r o l C,,H,,O (HENRY) 1624. 30 I11 DARD) 772. 1599. C,l Group. c32 Group. C3T Group. C,,H2,N, 37 I11 C,;H,,N,Cl Tri-3-c a r baz y 1 c a r b i n y 1 chloride (COPISAROW) 1546. C,,H,,ON Tr i-3-12 a r baz y I c a r b i n 01 ( COPISAROW) 1545. C31He40,N P h t h a 1 y l p h en y 1 t r i m e t h y 1 e n eb is h y d r azid e (CHATTAWAY and TEISH) 714. C,,H,,0sN4 4-&An t h r a q u i non e azo-1 &ant h r a q u i n o n yl-3-m e t h y 1-5-p y r-azolone (SAUNDERS) 1269. Tri-3-ca rbazylme t h a n e (COPISAROW) 1546. C38 Group. C,,H2, C,sH2,02N, 9 :9 10 1 O-T e t r a p h e n y 1-9:l O-d i h y d r o a n t h r a c e n c (RAY) 1339. 38 I11 c! a r b az o le-b 1 ue or Tr i-3-car baz y 1 c a r b i n y 1 form a t e (COPISA-EOW) 1546. C43 Group. C,,H,,N, C,,H3aN,C1 Tr i-9-e t h y 1 t ri-3-car baz y 1 c a r b i n y 1 c h l o r i d e (COPISAROW) 1548. C,,H,,ON T r i-9-e t !i y 1 t r i-3-ca r b a z y l c a r b i n o 1 (COPISAROW) 1549. Tri-9-e t h y 1 t r i-3-car b az y l m e t h a n e (COPIRAROW) 1548. 443 111 Cqp Group. C4,H,,02N C a r baz o le-v i o 1 e t or T r i-9-0 t h y 1 t ri-3.c a r baz y 1 c a r b i n y 1 for m-a t e (COPISAROW) 1547. 168