1416916-77-2

Basic information

• Product Name: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)benzenesulfonamide
• Synonyms: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)benzenesulfonamide
• CAS NO: 1416916-77-2
• Molecular Weight: 365.58
• Mol File: 1416916-77-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)benzenesulfonamide(1416916-77-2)
• EPA Substance Registry System: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)benzenesulfonamide(1416916-77-2)

Safety Data

• Hazardous Substances Data: 1416916-77-2(Hazardous Substances Data)

Upstream product

• 73604-46-3 2,2-dimethyl-1-amino-pent-4-ene 
• 57877-29-9 3,5-di-tert-butylbenzene-1-sulfonyl chloride 

Downstream Products

• 1416916-84-1 (S)-1-(1-((3,5-di-tert-butylphenyl)sulfonyl)-4,4-dimethylpyrrolidin-2-yl)methanol 
• 1416916-81-8 (S)-1-((1-((3,5-di-tert-butylphenyl)sulfonyl)-4,4-dimethylpyrrolidin-2-yl)methoxy)-2,2,6,6-tetramethylpiperidine 

Relevant articles and documents

Mechanistic analysis and optimization of the copper-catalyzed enantioselective intramolecular alkene aminooxygenation

The catalytic asymmetric aminooxygenation of alkenes provides an efficient and straightforward approach to prepare chiral vicinal amino alcohols. We have reported a copper(II)-catalyzed enantioselective intramolecular alkene aminooxygenation, using (2,2,6