13097-06-8

Usage

InChI:InChI=1/C10H8N2O2S2/c13-8-6-16-10(15)12(8)11-9(14)7-4-2-1-3-5-7/h1-5H,6H2,(H,11,14)

Upstream product

• 6326-83-6 bis(carboxymethyl)trithiocarbonate 
• 613-94-5 benzoic acid hydrazide 
• 3926-62-3 sodium monochloroacetic acid 
• 1438-16-0 3-aminorhodanine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 64145-06-8 (5-phenyl-1,3,4-thiadiazol-2-yl-sulfanyl)acetic acid 
• 24028-40-8 5-phenyl-1,3,4-thiadiazolin-2-one 
• 64145-13-7 (phenyl-[1,3,4]thiadiazol-2-ylmercapto)-acetic acid amide 
• 64145-10-4 (phenyl-[1,3,4]thiadiazol-2-ylmercapto)-acetic acid ethyl ester 
• 64145-14-8 (phenyl-[1,3,4]thiadiazole-2-sulfonyl)-acetic acid ethyl ester 
• 104064-03-1 {UO₂(C₃HNS(S)(O)(NHCOC₆H₅))2(CH₃OH)2} 
• 60126-72-9 5-methylsulfanyl-2-phenyl-thiazolo[4,3-b][1,3,4]thiadiazolylium; iodide 
• 60126-76-3 3-allyl-5-(2-phenyl-thiazolo[4,3-b][1,3,4]thiadiazol-5-ylidene)-2-thioxo-thiazolidin-4-one 
• 57639-63-1 2-phenyl-thiazolo[4,3-b][1,3,4]thiadiazole-5-thione 

Relevant academic research and scientific papers

Reaction of Carboxylic Acid Hydrazides with 2,2′-(Carbonothioyldisulfanediyl)diacetic acid in Water as a “Green” Synthesis of N-(4-Oxo-2-sulfanylidene-1,3-thiazolidin-3-yl) Carboxamides

Abstract: N-(4-Oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)benzamides were synthesized by reaction of substituted benzohydrazides with 2,2′-(carbonothioyldisulfanediyl)diacetic acid. Water was found to be the optimal reaction medium. The reaction conforms to

SAR and mode of action of novel non-nucleoside inhibitors of hepatitis C NS5b RNA polymerase

Novel non-nucleoside inhibitors of the HCV RNA polymerase (NS5b) with sub-micromolar biochemical potency have been identified which are selective for the inhibition of HCV NS5b over other polymerases. The structures of the complexes formed between several