372520-54-2

Basic information

• Product Name: (S)-2-Benzyloxycarbonylamino-3-(5-benzyloxy-1-oxy-pyridin-2-yl)-propionic acid methyl ester
• Synonyms: (S)-2-Benzyloxycarbonylamino-3-(5-benzyloxy-1-oxy-pyridin-2-yl)-propionic acid methyl ester
• CAS NO: 372520-54-2
• Molecular Weight: 436.464
• Mol File: 372520-54-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-Benzyloxycarbonylamino-3-(5-benzyloxy-1-oxy-pyridin-2-yl)-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-Benzyloxycarbonylamino-3-(5-benzyloxy-1-oxy-pyridin-2-yl)-propionic acid methyl ester(372520-54-2)
• EPA Substance Registry System: (S)-2-Benzyloxycarbonylamino-3-(5-benzyloxy-1-oxy-pyridin-2-yl)-propionic acid methyl ester(372520-54-2)

Safety Data

• Hazardous Substances Data: 372520-54-2(Hazardous Substances Data)

Upstream product

• 114684-69-4 methyl 2-(benzyloxycarbonylamino)-2-(diethyloxyphosphoryl)acetate 
• 100945-15-1 N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester 
• 59781-11-2 (5-(benzyloxy)pyridin-2-yl)methanol 
• 59781-08-7 5-benzyloxypyridin-2-carbaldehyde 

Downstream Products

• 372520-55-3 (S)-2-Benzyloxycarbonylamino-3-(5-benzyloxy-pyridin-2-yl)-propionic acid methyl ester 
• 58525-82-9 L-azatyrosine 

Relevant articles and documents

Enantioselective synthesis of (2-pyridyl)alanines via catalytic hydrogenation and application to the synthesis of L-azatyrosine.

[reaction: see text] A novel method for the synthesis of (2-pyridyl)alanines 2a-b was developed by converting (2-pyridyl)dehydroamino acid derivatives 1a-b to the corresponding N-oxides 3a-b followed by asymmetric hydrogenation using (R,R)-[Rh(Et-DUPHOS)(