23837-25-4

Basic information

• Product Name: Benzenesulfenamide, N-butyl-
• CAS NO: 23837-25-4
• Molecular Formula: C10H15NS
• Molecular Weight: 181.302
• Mol File: 23837-25-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenesulfenamide, N-butyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfenamide, N-butyl-(23837-25-4)
• EPA Substance Registry System: Benzenesulfenamide, N-butyl-(23837-25-4)

Safety Data

• Hazardous Substances Data: 23837-25-4(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 109-73-9 N-butylamine 
• 4972-29-6 benzenesulphinyl chloride 
• 931-59-9 benzenesulfenyl chloride 
• 28715-70-0 methoxy-phenyl-sulfane 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 139-66-2 diphenyl sulfide 
• 33932-80-8 4-(methylthio)phenyl phenyl sulfide 
• 54815-65-5 2-(methylthio)phenyl phenyl sulfide 
• 882-33-7 diphenyldisulfane 
• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 92-52-4 biphenyl 
• 6829-66-9 N-butylbenzenesulfinamide 
• 3622-84-2 N-butylbenzenesulfonamide 

Relevant articles and documents

Copper-catalyzed synthesis of sulfenamides utilizing diaryl disulfides with alkyl amines

The copper-catalyzed coupling of diaryl disulfides with alkyl amines can afford various sulfenamides in good yields. Furthermore, the present reaction is efficient and can be used for both of the aryl sulfide groups on disulfide. Georg Thieme Verlag Stutt

Copper-catalyzed formation of sulfur-nitrogen bonds by dehydrocoupling of thiols with amines

Copper-catalyzed formation of sulfur-nitrogen bonds can be performed by a dehydrocoupling of aryl thiols with amines. Sulfenamides or sulfonamides can be produced by the use of a copper catalyst in air or under oxygen atmosphere. Furthermore, a reaction involving the combination of a palladium catalyst and a copper catalyst selectively afforded sulfinamides.