60199-42-0

Basic information

• Product Name: p-nitrobenzoyl-(N-benzoyl)-iminosulfinyl chloride
• Synonyms: p-nitrobenzoyl-(N-benzoyl)-iminosulfinyl chloride
• CAS NO: 60199-42-0
• Molecular Weight: 308.745
• Mol File: 60199-42-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: p-nitrobenzoyl-(N-benzoyl)-iminosulfinyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: p-nitrobenzoyl-(N-benzoyl)-iminosulfinyl chloride(60199-42-0)
• EPA Substance Registry System: p-nitrobenzoyl-(N-benzoyl)-iminosulfinyl chloride(60199-42-0)

Safety Data

• Hazardous Substances Data: 60199-42-0(Hazardous Substances Data)

Upstream product

• 111680-13-8 C₁₈H₁₈N₄O₈S₂ 
• 101414-54-4 ethyl N-(p-nitrophenylthio)benzenecarboximidate 
• 33243-83-3 N-chloro-benzimidic acid ethyl ester 
• 1011-57-0 N-trimethylsilylbenzamide 
• 60199-37-3 N-benzoyl p-nitrobenzenesulfenamide 
• 937-32-6 4-nitrobenzenesulfenyl chloride 
• 1821-34-7 N-chlorobenzamide 
• 101414-51-1 N-amino(p-nitrophenyl)dichlorosulfurane 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 54858-85-4 N-chloro-benzimidic acid methyl ester 

Downstream Products

• 83102-59-4 N,N'-dibenzoyl-N-(p-chlorophenylthio)-p-chlorophenylsulfinamidine 
• 83102-57-2 N,N-di-(p-chlorophenylthio)benzamide 
• 67302-30-1 3-(4-nitro-phenylsulfanyl)-pentane-2,4-dione 
• 18513-03-6 N-Benzoyl-p-nitrobenzolsulfinsaeureamid 
• 60199-37-3 N-benzoyl p-nitrobenzenesulfenamide 
• 933-01-7 4-chloro-benzenesulfenyl chloride 

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.