89879-95-8

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-[(4-methylphenyl)sulfonyl]-N-(5-phenyl-1,2,4-thiadiazol-3-yl)-
• CAS NO: 89879-95-8
• Molecular Formula: C22H19N3O4S3
• Molecular Weight: 485.609
• Mol File: 89879-95-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-[(4-methylphenyl)sulfonyl]-N-(5-phenyl-1,2,4-thiadiazol-3-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[(4-methylphenyl)sulfonyl]-N-(5-phenyl-1,2,4-thiadiazol-3-yl)-(89879-95-8)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[(4-methylphenyl)sulfonyl]-N-(5-phenyl-1,2,4-thiadiazol-3-yl)-(89879-95-8)

Safety Data

• Hazardous Substances Data: 89879-95-8(Hazardous Substances Data)

Upstream product

• 89880-02-4 N-carbamoyl-N'-thiobenzoylguanidine 
• 7746-72-7 N¹-benzoyl-N³-cyanoguanidine 
• 27182-54-3 5-phenyl-1,2,4-thiadiazol-3-amine 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Cyclic Meso-ionic Compounds. Part 23. Novel Chemistry of 1,2,4-Thiadiazoles and Their Transformation into Meso-ionic 1,2,4-Thiadiazolium Derivatives

Representatives of two new classes of meso-ionic heterocycles have been synthesised, the 1,2,4-thiadiazolium-3-olate (8) and the 1,2,4-thiadiazolium-3-tosylaminide (25).The reactions of 1,2,4-thiadiazoles and nucleophiles follow two general pathways: (i) reductive transformation to N-thiobenzoyl derivatives and (ii) elimination of elemental sulphur and the formation of N-benzoyl derivatives.A mechanistic rationale is proposed for the operation of pathways (i) and (ii).Earlier views on the oxidative formation of certain 1,2,4-thiadiazoles are corrected.A novel synthetic route to heterocycles containing sulphur-nitrogen bonds is described. 1,2,4-Thiadiazoles are formed by oxidation of N-thiobezoylureas and N-thiobenzoylguanidines by bis(4-methoxyphenyl) telluroxide.