235089-84-6

Basic information

• Product Name: (R)-2-Benzylamino-4-phenyl-butyric acid methyl ester
• Synonyms: (R)-2-Benzylamino-4-phenyl-butyric acid methyl ester
• CAS NO: 235089-84-6
• Molecular Weight: 283.37
• Mol File: 235089-84-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-2-Benzylamino-4-phenyl-butyric acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-Benzylamino-4-phenyl-butyric acid methyl ester(235089-84-6)
• EPA Substance Registry System: (R)-2-Benzylamino-4-phenyl-butyric acid methyl ester(235089-84-6)

Safety Data

• Hazardous Substances Data: 235089-84-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 235089-83-5 N-benzyl-2-nitro-N-(1-phenethyl-allyl)-benzenesulfonamide 
• 42060-32-2 N-benzyl-2-nitrobenzenesulfonamide 
• 82795-51-5 D-homophenylalanine 
• 100-39-0 benzyl bromide 
• 139891-43-3 2-(R)-amino-4-phenylbutyric acid methyl ester 

Downstream Products

• 82795-51-5 D-homophenylalanine 
• 139891-43-3 2-(R)-amino-4-phenylbutyric acid methyl ester 

Relevant articles and documents

Controlling diastereoselectivity in the reactions of enantiomerically pure α-bromoacyl-imidazolidinones with nitrogen nucleophiles: Substitution reactions with retention or inversion of configuration

Diastereoselective substitution reactions of α-bromoacyl- imidazolidinones with nitrogen nucleophiles can be promoted with either retention or inversion of configuration by carrying out reactions under epimerising or non-epimerising conditions. The Royal Society of Chemistry 2005.