1237829-23-0

Basic information

• Product Name: (R)-N-(4-((1-bromo-2-(4-methyl-5-oxocyclohex-3-en-1-yl)propan-2-yl)oxy)butyl)-4-nitrobenzenesulfonamide
• CAS NO: 1237829-23-0
• Molecular Weight: 503.414
• Mol File: 1237829-23-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-N-(4-((1-bromo-2-(4-methyl-5-oxocyclohex-3-en-1-yl)propan-2-yl)oxy)butyl)-4-nitrobenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-N-(4-((1-bromo-2-(4-methyl-5-oxocyclohex-3-en-1-yl)propan-2-yl)oxy)butyl)-4-nitrobenzenesulfonamide(1237829-23-0)
• EPA Substance Registry System: (R)-N-(4-((1-bromo-2-(4-methyl-5-oxocyclohex-3-en-1-yl)propan-2-yl)oxy)butyl)-4-nitrobenzenesulfonamide(1237829-23-0)

Safety Data

• Hazardous Substances Data: 1237829-23-0(Hazardous Substances Data)

Upstream product

• 109-99-9 tetrahydrofuran 
• 6485-40-1 (R)-Carvone 
• 6325-93-5 p-nitrobenzenesulfonamide 

Relevant articles and documents

Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application

A new one-pot electrophilic aminoalkoxylation reaction using olefin, cyclic ether, amine, and N-bromosuccinimide has been developed. The olefinic substrates and the cyclic ether partners can be flexibly varied to produce a range of amino ether derivatives. This novel protocol has been applied in the facile and efficient synthesis of biologically active morpholine compounds.