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The preparation of symmetric and asymmetric aminopropanediol and of some of their derivatives

 

作者: H. P. den Otter,  

 

期刊: Recueil des Travaux Chimiques des Pays‐Bas  (WILEY Available online 1938)
卷期: Volume 57, issue 1  

页码: 13-24

 

ISSN:0165-0513

 

年代: 1938

 

DOI:10.1002/recl.19380570103

 

出版商: WILEY‐VCH Verlag

 

数据来源: WILEY

 

摘要:

AbstractIn the following workPart of a dissertation.) the derivatives are described which were obtained when 2‐aminopropanediol‐1,3 and 3‐aminopropanediol‐1,2 were coupled with aromatic nitro‐compounds containing a substitutive chlorine atom such as 1‐chloro‐2,4‐dinitrobenzene, 1‐chloro‐2,4,6‐trinitrobenzene, 1‐chloro‐2,4‐dinitronaphthalene and 1,3‐dichloro‐4,6‐dinitrobenzene. On nitration, the substances thus obtained gave explosive compounds which were comparable with a combination of trinitrophenylmethylnitramine (tetryl) and nitroglycerine.For comparison, the attempt has been made to couple d. glucosamine with aromatic halogen‐nitro‐compounds, an

 

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