660838-99-3

Basic information

• Product Name: methyl (E,S)-2-(4-methoxybenzylideneamino)-3-phenylpropionate
• Synonyms: methyl (E,S)-2-(4-methoxybenzylideneamino)-3-phenylpropionate
• CAS NO: 660838-99-3
• Molecular Weight: 297.354
• Mol File: 660838-99-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl (E,S)-2-(4-methoxybenzylideneamino)-3-phenylpropionate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (E,S)-2-(4-methoxybenzylideneamino)-3-phenylpropionate(660838-99-3)
• EPA Substance Registry System: methyl (E,S)-2-(4-methoxybenzylideneamino)-3-phenylpropionate(660838-99-3)

Safety Data

• Hazardous Substances Data: 660838-99-3(Hazardous Substances Data)

Upstream product

• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 53933-45-2 (S)-1-Methoxycarbonyl-2-phenylethylhydroxylamine 
• 73995-67-2 (S)-2-[3-(4-Methoxy-phenyl)-oxaziridin-2-yl]-3-phenyl-propionic acid methyl ester 

Relevant articles and documents

Synthesis of chiral azomethines from methyl l-3-phenylalaninate hydrochloride and substituted benzaldehydes of vanillin series

A preparative procedure is developed for the synthesis of chiral azomethines from methyl L-3-phenylalaninate and substituted aldehydes of vanillin series.

Process for producing alpha-aminoketones

An amino group of an α-amino acid ester is protected as an imine, and it is then reacted with a halomethyllithium to obtain an N-protected-α-aminohalomethylketone. Further, this N-protected-α-aminohalomethylketone is treated with an acid to obtain an α-aminohalomethylketone. This process is suited for industrial production, and can produce an α-aminohalomethylketone and its related compounds economically and efficiently.