154777-31-8

Basic information

• Product Name: cis-N-(benzenesulfenyl)-5-(4-isopropylphenyl)pent-4-enylamine
• Synonyms: cis-N-(benzenesulfenyl)-5-(4-isopropylphenyl)pent-4-enylamine
• CAS NO: 154777-31-8
• Molecular Weight: 311.491
• Mol File: 154777-31-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: cis-N-(benzenesulfenyl)-5-(4-isopropylphenyl)pent-4-enylamine(CAS DataBase Reference)
• NIST Chemistry Reference: cis-N-(benzenesulfenyl)-5-(4-isopropylphenyl)pent-4-enylamine(154777-31-8)
• EPA Substance Registry System: cis-N-(benzenesulfenyl)-5-(4-isopropylphenyl)pent-4-enylamine(154777-31-8)

Safety Data

• Hazardous Substances Data: 154777-31-8(Hazardous Substances Data)

Upstream product

• 931-59-9 benzenesulfenyl chloride 
• 154777-52-3 cis-4-cyano-1-(4-isopropylphenyl)but-1-ene 
• 603-35-0 triphenylphosphine 
• 108-98-5 thiophenol 
• 7752-62-7 3-cyanopropyltriphenylphosphonium bromide 
• 14204-27-4 N-phenylthiophthalimide 
• 154777-53-4 cis-5-(4-isopropylphenyl)pent-4-enylamine 

Relevant articles and documents

Generation of Aminyl Radicals using Sulfenamides as Synthetic Precursors

Sulfenamides are synthesised from reaction between amines and N-(benzenesulfenil)-phthalimide or benzenesulfenyl chloride.The sulfenamides undergo reaction with tributyltin hydride to yield aminyl radicals which can be cyclised onto suitable alkenes. Key Words: sulfenamides; aminyl radicals; tributyltin hydride; radical-cyclisation; N-(benzenesulfenyl)phthalimide