Author:
Dalton JR,Kirkpatrick A,Maclaren JA
Abstract
A series of thiol esters,
and S-esters of thiocarbamic acid,
has been prepared by making mercapto-acetic acid or 2-mercaptoethanesulfonic
acid react with carboxylic acid chlorides or with isocyanates. Aqueous
solutions of these products are stable to hydrolysis but rapidly acylate
amines. Azo-dyes that incorporate these reactive groups have been synthesized.
Cited by
1 articles.
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1. Guanidinium 2-(myristoylsulfanyl)ethanesulfonate;Acta Crystallographica Section E Structure Reports Online;2011-11-12