39549-16-1

Basic information

• Product Name: N-Acetyl-p-nitrobenzenesulfenamide
• Synonyms: N-Acetyl-p-nitrobenzenesulfenamide
• CAS NO: 39549-16-1
• Molecular Weight: 212.229
• Mol File: 39549-16-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-Acetyl-p-nitrobenzenesulfenamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Acetyl-p-nitrobenzenesulfenamide(39549-16-1)
• EPA Substance Registry System: N-Acetyl-p-nitrobenzenesulfenamide(39549-16-1)

Safety Data

• Hazardous Substances Data: 39549-16-1(Hazardous Substances Data)

Upstream product

• 60-35-5 acetamide 
• 937-32-6 4-nitrobenzenesulfenyl chloride 
• 598-49-2 N-chloroacetamide 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 1849-36-1 para-nitrobenzenethiol 

Downstream Products

• 1041-15-2 p-nitrophenyl p-nitrobenzenethiosulfonate 
• 88951-70-6 N,N'-diacetyl-p-nitrobenzenesulfinamidine 
• 105897-00-5 C₈H₇N₂O₃S^(1-)*Na⁽¹⁺⁾ 
• 74448-86-5 N-acetyl-N'-phenylsulfonyl-4-nitrobenzenesulfinamidine 
• 18112-84-0 N,N'-bis(phenylsulfonyl)-p-nitrobenzenesulfinamidine 

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.