79561-72-1

Basic information

• Product Name: N,N-bis-allyl-L-phenylalanine methyl ester
• Synonyms: N,N-bis-allyl-L-phenylalanine methyl ester
• CAS NO: 79561-72-1
• Molecular Weight: 259.348
• Mol File: 79561-72-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N,N-bis-allyl-L-phenylalanine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-bis-allyl-L-phenylalanine methyl ester(79561-72-1)
• EPA Substance Registry System: N,N-bis-allyl-L-phenylalanine methyl ester(79561-72-1)

Safety Data

• Hazardous Substances Data: 79561-72-1(Hazardous Substances Data)

Upstream product

• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 106-95-6 allyl bromide 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 

Downstream Products

• 847899-98-3 (S)-methyl 2-(2,5-dihydro-1H-pyrrol-1-yl)-3-phenylpropanoate 
• 116763-08-7 methyl (S)-3-phenyl-2-(1H-pyrrol-1-yl)propanoate 
• 890657-45-1 2-diallylamino-3-phenyl-propionic acid N'-phenyl-hydrazide 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 

Relevant articles and documents

Synthesis of enantiomerically pure (+)- and (-)-protected 5-aminomethyl-1,3-oxazolidin-2-one derivatives from allylamine and carbon dioxide

The stereoselective synthesis of enantiomerically pure (5R)- and (5S)-aminomethyl-oxazolidinones with different protecting groups have been carried out from an allyl amine as the source of the carbon backbone. The key reaction is the high yield iodiocyclization of enantiomerically pure allylphenethyl amine in the presence of carbon dioxide.

A NEW PROTECTING GROUP FOR AMINES. SYNTHESIS OF ANTICAPSIN FROM L-TYROSINE

An acid and base-stable, nucleophile-resistant protecting group for primary amines and α-amino acids is described which has been used in a synthesis of the title compound.