909713-17-3

Basic information

• Product Name: (R)-2-(4-Methoxy-benzylamino)-4-phenyl-butyric acid methyl ester
• CAS NO: 909713-17-3
• Molecular Weight: 313.397
• Mol File: 909713-17-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2-(4-Methoxy-benzylamino)-4-phenyl-butyric acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-(4-Methoxy-benzylamino)-4-phenyl-butyric acid methyl ester(909713-17-3)
• EPA Substance Registry System: (R)-2-(4-Methoxy-benzylamino)-4-phenyl-butyric acid methyl ester(909713-17-3)

Safety Data

• Hazardous Substances Data: 909713-17-3(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 139891-43-3 2-(R)-amino-4-phenylbutyric acid methyl ester 

Downstream Products

• 909713-25-3 (4S)-1-(p-methoxy)benzyl-4-phenethyl-4-methoxycarbonyl-2-azetidinone 
• 909713-36-6 (4R)-1-(p-methoxy)benzyl-4-phenethyl-4-methoxycarbonyl-2-azetidinone 
• 909713-22-0 (R)-2-[(2-Chloro-acetyl)-(4-methoxy-benzyl)-amino]-4-phenyl-butyric acid methyl ester 

Relevant articles and documents

β-Lactams derived from phenylalanine and homologues: effects of the distance between the aromatic rings and the α-stereogenic reactive center on the memory of chirality

The enantioselectivity in the base-promoted cyclization of N-chloroacetyl derivatives of Phe, Phg, and Hph is dependent on the side-chain length, with the best results for Phg analogues (up to 74% ee). In contrast, shortening of the N-substituent, from a