39031-43-1

Upstream product

• 121-66-4 2-amino-5-nitro-1,3-thiazole 
• 1885-14-9 phenyl chloroformate 

Downstream Products

• 38922-60-0 [5-nitro-3-(2-oxo-2-piperidin-1-yl-ethyl)-3H-thiazol-2-ylidene]-carbamic acid phenyl ester 
• 38922-57-5 [3-(diethylcarbamoyl-methyl)-5-nitro-3H-thiazol-2-ylidene]-carbamic acid phenyl ester 
• 38922-58-6 [3-(dipropylcarbamoyl-methyl)-5-nitro-3H-thiazol-2-ylidene]-carbamic acid phenyl ester 
• 38922-59-7 [3-(dibutylcarbamoyl-methyl)-5-nitro-3H-thiazol-2-ylidene]-carbamic acid phenyl ester 
• 38922-61-1 N-(5-nitro-thiazol-2-yl)-N-phenoxycarbonyl-glycine ethyl ester 

Relevant academic research and scientific papers

Mechanism of hydrolysis of substituted N-thiazolylcarbamate esters in OH- solutions

Substituted secondary N-thiazolylcarbamate esters and some tertiary N-methyl, N-thiazolyl carbamate esters have been synthesised and the mechanism of the OH- catalysed hydrolyses investigated. These proved to be E1cB and BAc2 respectively, and this behaviour was compared with that of other carbamates.