7449-47-0

Basic information

• Product Name: Benzenesulfonic acid, 4-methyl-, 2-(aminothioxomethyl)hydrazide
• CAS NO: 7449-47-0
• Molecular Formula: C8H11N3O2S2
• Molecular Weight: 245.326
• Mol File: 7449-47-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonic acid, 4-methyl-, 2-(aminothioxomethyl)hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonic acid, 4-methyl-, 2-(aminothioxomethyl)hydrazide(7449-47-0)
• EPA Substance Registry System: Benzenesulfonic acid, 4-methyl-, 2-(aminothioxomethyl)hydrazide(7449-47-0)

Safety Data

• Hazardous Substances Data: 7449-47-0(Hazardous Substances Data)

Upstream product

• 79-19-6 thiosemicarbazide 
• 98-59-9 p-toluenesulfonyl chloride 
• 2092-17-3 barium thiocyanate 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 

Downstream Products

• 527715-78-2 4-phenyl-2-[2-(p-toluenesulfonyl)-hydrazino]-thiazole 
• 1256585-57-5 5-acetyl-4-methyl-2-[2-(p-toluenesulfonyl)-hydrazino]-thiazole 
• 1256585-54-2 4-chloromethyl-2-[2-(p-toluenesulfonyl)-hydrazino]-thiazole 
• 528887-25-4 4-methyl-2-[2-(p-toluenesulfonyl)-hydrazino]-thiazole 
• 1256585-61-1 ethyl (2-[2-(p-toluenesulfonyl)-hydrazino]-thiazol-4-yl)acetate 
• 1256585-59-7 5-ethoxycarbonyl-4-methyl-2-[2-(p-toluenesulfonyl)-hydrazino]-thiazole 
• 93283-02-4 1-p-Toluolsulfonyl-S-methyl-isothiosemicarbazid 
• 16019-18-4 N,N,N'-Tris-(2-cyan-aethyl)-N'-p-toluolsulfonylhydrazin 

Relevant articles and documents

Sulfonamide-Linked ciprofloxacin, sulfadiazine and amantadine derivatives as a novel class of inhibitors of jack bean urease; synthesis, kinetic mechanism and molecular docking

Sulfonamide derivatives serve as an important building blocks in the drug design discovery and development (4D) process. Ciprofloxacin-, sulfadiazine- and amantadine-based sulfonamides were synthesized as potent inhibitors of jack bean urease and free rad

CARBONIC ANHYDRASE INHIBITORS. 9. INHIBITORS WITH MODIFIED SULFONAMIDO GROUPS AND THEIR INTERACTION WITH THE ZINC ENZYME

A number of 20 compounds, containing modified sulfonamido groups were prepared and tested as carbonic anhydrase inhibitors on the bovine enzyme. Novel classes of inhibitors were evidenced, and a new mode of binding for bidentate inhibitors was proposed, both for the native and Co(II) substituted enzyme.