112302-89-3

Basic information

• Product Name: DL-Phenylalanine, N,N-bis(phenylmethyl)-, methyl ester
• CAS NO: 112302-89-3
• Molecular Formula: C24H25NO2
• Molecular Weight: 359.468
• Mol File: 112302-89-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: DL-Phenylalanine, N,N-bis(phenylmethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: DL-Phenylalanine, N,N-bis(phenylmethyl)-, methyl ester(112302-89-3)
• EPA Substance Registry System: DL-Phenylalanine, N,N-bis(phenylmethyl)-, methyl ester(112302-89-3)

Safety Data

• Hazardous Substances Data: 112302-89-3(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 112302-87-1 2-dibenzylaminopropionic acid methyl ester 
• 57956-49-7 {(1-methoxy-3-phenylprop-1-en-1-yl)oxy}trimethylsilane 
• 52742-32-2 N,N-dibenzyl-O-benzoylhydroxylamine 
• 94226-55-8 (dibenzylamino)acetic acid methyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 398487-97-3 C₂₃H₂₂⁽²⁾HNO 
• 398488-07-8 C₂₃H₂₂NO⁽²⁾H₂H 
• 5619-07-8 methyl 2-amino-3-phenylpropanoate hydrochloride 

Relevant articles and documents

An umpolung-enabled copper-catalysed regioselective hydroamination approach to α-amino acids

A copper-catalysed regio- and stereoselective hydroamination of acrylates with hydrosilanes and hydroxylamines has been developed to afford the corresponding α-amino acids in good yields. The key to regioselectivity control is the use of hydroxylamine as

Synthesis of aromatic α-aminoesters: Palladium-catalyzed long-range arylation of primary Csp3-H bonds

Remote control: The title reaction for β-Iζ arylation of α-amino esters with aryl bromides is described. This reaction, which occurs selectively at the terminal position of linear alkyl chains, gives rise to synthetically useful (hetero)arylalanines and homologues after debenzylation (see scheme). Copyright