767239-17-8

Basic information

• Product Name: L-Alanine, N-hydroxy-, ethyl ester (9CI)
• Synonyms: L-Alanine, N-hydroxy-, ethyl ester (9CI)
• CAS NO: 767239-17-8
• Molecular Formula: C5H11NO3
• Molecular Weight: 133.14574
• Product Categories: GLYCINESCAFFOLD
• Mol File: 767239-17-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: L-Alanine, N-hydroxy-, ethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-hydroxy-, ethyl ester (9CI)(767239-17-8)
• EPA Substance Registry System: L-Alanine, N-hydroxy-, ethyl ester (9CI)(767239-17-8)

Safety Data

• Hazardous Substances Data: 767239-17-8(Hazardous Substances Data)

Upstream product

• 1462968-79-1 (S,Z)-N-(1-ethoxy-1-oxopropan-2-yl)-1-phenylmethanimine oxide 
• 60855-77-8 ethyl N-benzylidenealaninate 

Downstream Products

• 1462968-91-7 methyl (3R,5R)-2-((S)-1-ethoxy-1-oxopropan-2-yl)-3-phenylisoxazolidine-5-carboxylate 
• 1462968-79-1 (S,Z)-N-(1-ethoxy-1-oxopropan-2-yl)-1-phenylmethanimine oxide 
• 1462968-80-4 (S,Z)-N-(1-ethoxy-1-oxopropan-2-yl)-1-(furan-2-yl)methanimine oxide 
• 1462968-93-9 methyl (3R,5R)-3-((benzyloxy)methyl)-2-((S)-1-ethoxy-1-oxopropan-2-yl)isoxazolidine-5-carboxylate 
• 1462968-81-5 (S,Z)-2-(benzyloxy)-N-(1-ethoxy-1-oxopropan-2-yl)ethan-1-imine oxide 
• 1462969-02-3 (3R,5R)-1-((S)-1-ethoxy-1-oxopropan-2-yl)-5-isopropyl-2-oxopyrrolidin-3-yl (R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 
• 1462969-04-5 (3R,5R)-1-((S)-1-ethoxy-1-oxopropan-2-yl)-5-isopropyl-2-oxopyrrolidin-3-yl (S)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 

Relevant articles and documents

Stereoselective 1,3-dipolar cycloadditions of nitrones derived from amino acids. Asymmetric synthesis of N-(alkoxycarbonylmethyl)-3-hydroxypyrrolidin-2- ones Dedicated to Professor Giovanni Romeo on occasion of his 70th birthday

Diastereoselective asymmetric 1,3-dipolar cycloadditions of N-(alkoxycarbonylmethyl) nitrones derived from glycine, alanine and phenylalanine have been studied both experimentally and theoretically. Asymmetric induction is evaluated by either introducing