71151-37-6

Basic information

• Product Name: p-chlorobenzene(N-benzoyl)iminosulfinyl chloride
• Synonyms: p-chlorobenzene(N-benzoyl)iminosulfinyl chloride
• CAS NO: 71151-37-6
• Molecular Weight: 298.193
• Mol File: 71151-37-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: p-chlorobenzene(N-benzoyl)iminosulfinyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: p-chlorobenzene(N-benzoyl)iminosulfinyl chloride(71151-37-6)
• EPA Substance Registry System: p-chlorobenzene(N-benzoyl)iminosulfinyl chloride(71151-37-6)

Safety Data

• Hazardous Substances Data: 71151-37-6(Hazardous Substances Data)

Upstream product

• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 1821-34-7 N-chlorobenzamide 
• 68556-47-8 N-benzoyl-p-chlorobenzenesulfenamide 
• 55-21-0 benzamide 
• 933-01-7 4-chloro-benzenesulfenyl chloride 
• 81386-74-5 C₂₀H₁₅ClN₂O₂S 
• 33243-83-3 N-chloro-benzimidic acid ethyl ester 
• 54858-85-4 N-chloro-benzimidic acid methyl ester 

Downstream Products

• 81386-74-5 N,N'-dibenzoyl-p-chlorobenzenesulfinamidine 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 83102-57-2 N,N-di-(p-chlorophenylthio)benzamide 
• 83102-59-4 N,N'-dibenzoyl-N-(p-chlorophenylthio)-p-chlorophenylsulfinamidine 
• 15934-46-0 benzamidene hydrochloride 
• 83102-60-7 N,N'-dibenzoyl-N-(p-methylphenylthio)-N-methylphenylsulfinamidine 

Relevant articles and documents

REACTION OF DIARYL DISULFIDES WITH N-CHLOROBENZENECARBOXIMIDIC AND N-CHLOROCARBONIMIDIC ESTERS

Diaryl disulfides and alkyl N-chlorobenzenecarboximidates react in a molar ratio of 1:2 with the formation of alkyl N-(arylthio)benzenecarboximidates and N-benzoylarenesulfinimidoyl chlorides.The reaction of diaryl disulfides with ethyl N-chlorocarbonimidate gives N,N'-bis(arylthio)-N,N'-bis(ethoxycarbonyl)hydrazines.

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.