70925-53-0

Basic information

• Product Name: p-toluene(N-benzoyl)iminosulfinyl chloride
• Synonyms: p-toluene(N-benzoyl)iminosulfinyl chloride
• CAS NO: 70925-53-0
• Molecular Weight: 277.774
• Mol File: 70925-53-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-toluene(N-benzoyl)iminosulfinyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: p-toluene(N-benzoyl)iminosulfinyl chloride(70925-53-0)
• EPA Substance Registry System: p-toluene(N-benzoyl)iminosulfinyl chloride(70925-53-0)

Safety Data

• Hazardous Substances Data: 70925-53-0(Hazardous Substances Data)

Upstream product

• 933-00-6 p-methylbenzenesulfenyl chloride 
• 1821-34-7 N-chlorobenzamide 

Downstream Products

• 103-19-5 di(p-tolyl) disulfide 
• 83102-58-3 N,N-di(p-tolylthio)-benzamide 
• 83102-60-7 N,N'-dibenzoyl-N-(p-methylphenylthio)-N-methylphenylsulfinamidine 
• 15934-46-0 benzamidene hydrochloride 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 83102-59-4 N,N'-dibenzoyl-N-(p-chlorophenylthio)-p-chlorophenylsulfinamidine 

Relevant articles and documents

OXIDATION IMINATION OF SULFENYL CHLORIDES BY N-CHLOROCARBOXAMIDES. N-ACYLSULFINIMIDOYL CHLORIDES

The reaction of arenesulfenyl chlorides ArSCl with N-chlorocarboxyamides in a ratio of 1:1 leads to the formation of N-acylsulfinimidoyl chlorides ArS(=NCOR)Cl.The reaction of arenesulfenyl chlorides and N-chlorobenzamide in ratio of 1:1 leads to aryldibenzamidosulfonium chlorides ArS(NHCOC6H5)2, which are hydrolyzed with the formation of N,N'-benzoylarenesulfinamidines ArS(=NCOC6H5)NHCOC6H5 and are cleaved into acid chlorides and benzamide when heated.