305647-06-7

Basic information

• Product Name: (S)-3-tert-Butoxy-2-[(E)-3-(3-phenoxy-phenyl)-allylamino]-propionic acid methyl ester
• CAS NO: 305647-06-7
• Molecular Weight: 383.488
• Mol File: 305647-06-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-3-tert-Butoxy-2-[(E)-3-(3-phenoxy-phenyl)-allylamino]-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-tert-Butoxy-2-[(E)-3-(3-phenoxy-phenyl)-allylamino]-propionic acid methyl ester(305647-06-7)
• EPA Substance Registry System: (S)-3-tert-Butoxy-2-[(E)-3-(3-phenoxy-phenyl)-allylamino]-propionic acid methyl ester(305647-06-7)

Safety Data

• Hazardous Substances Data: 305647-06-7(Hazardous Substances Data)

Upstream product

• 17083-26-0 O-tert-butyl-L-serine methyl ester 
• 112270-87-8 E-3-(3-phenoxyphenyl)-1-bromoprop-2-ene 

Downstream Products

• 305647-10-3 (S)-3-Hydroxy-2-[(E)-3-(3-phenoxy-phenyl)-allylamino]-propionic acid methyl ester 

Relevant articles and documents

Synthesis and erythropoietin receptor binding affinities of N, N-disubstituted amino acids

N,N-Dicinnamyl, N-benzyl-N-cinnamyl, and N,N-dibenzyl amino acids were prepared and evaluated in an EPO binding assay. Several derivatives of aspartic acid, glutamic acid, and lysine exhibited moderate (10-50 μM) affinity for EBP; 'dimerization' of the most potent analogues by coupling with linear diamines led to EPO competitors having 1-2 μM binding affinities. (C) 2000 Elsevier Science Ltd.