2651-13-0

Upstream product

• 75-15-0 carbon disulfide 
• 121-61-9 p-acetylaminobenzenesulfonamide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 25046-66-6 2-(p-acetylaminobenzenesulphonylimino)imidazoline 
• 149992-61-0 N-[4-(1,3-Dihydro-benzoimidazol-2-ylidenesulfamoyl)-phenyl]-acetamide 
• 2733-54-2 4-amino-N-(4,5-dihydro-1H-imidazol-2-yl)-benzenesulfonamide 
• 52715-11-4 4-amino-N-(1,3-dihydrobenzoimidazol-2-ylidene)benzenesulfonamide 
• 149992-63-2 4-Amino-N-oxazolidin-(2Z)-ylidene-benzenesulfonamide 
• 149992-62-1 1-(p-aminobenzenesulfonyl)-2-mercaptomethyl-3-(phenyl ethyl) formamidine 
• 2800-78-4 1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea 
• 2718-35-6 N-(4-amino-benzenesulfonyl)-morpholine-4-carboximidothioic acid methyl ester 

Relevant academic research and scientific papers

Syhthesis of N4-substituted sulphanilamides and evaluation of their antibacterial efficacy

Pharmacologically active compounds belonging to the classes of p-thiocyano and p-aminobenzene sulphonamides have been synthesised and their antimicrobial activity evaluated against Gram + ve and Gram - ve bacteria.The compounds of both the classes show more inhibition of Gram -ve bacteria as compared to Gram + ve.

Regiospecific synthesis of N-sulfonyl derivatives of 3,5-diamino-1H-1,2,4-triazole and 2,5-diamino-1,3,4-thiadiazole

Condensation of the S,S-dimethyl N-(alkylsulfonyl)carbondithioimidates 1 with aminoguanidine bicarbonate and hydrazinecarbothioamide leads to the regiospecific synthesis of N-sulfonyl derivatives of 3,5-diamino-1H-1,2,4-triazole 2 and 2,5-diamino-1,3,4-thiadiazole 3, respectively.