3209-39-0

Basic information

• Product Name: 2-amino-4-hydroxypentanoic acid
• Synonyms: 2-amino-4-hydroxypentanoic acid
• CAS NO: 3209-39-0
• Molecular Weight: 133.147
• Mol File: 3209-39-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-amino-4-hydroxypentanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-hydroxypentanoic acid(3209-39-0)
• EPA Substance Registry System: 2-amino-4-hydroxypentanoic acid(3209-39-0)

Safety Data

• Hazardous Substances Data: 3209-39-0(Hazardous Substances Data)

Upstream product

• 129519-79-5 (+)-(3R,5R)-3-Azido-5-methyldihydro-2(3H)-furanone 
• 96291-06-4 (3R,4S,5R)-3,4-dihydroxy-5-methyldihydrofuran-2-one 
• 208461-51-2 (+)-(3R,5R)-3-Amino-5-methyldihydro-2(3H)-furanone hydrochloride 
• 135263-84-2 (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl (2S)-2-<(tert-butoxycarbonyl)amino>pent-4-enoate 
• 2833-28-5 trans-4-oxo-2-pentenoic acid 
• 129453-36-7 (-)-2-O-Tosyl-5-deoxy-γ-D-ribonolactone 
• 129453-38-9 (+)-(3S,5R)-3-Tosyloxy-5-methyldihydro-2(3H)-furanone 
• 129453-37-8 (-)-(R)-3-Tosyloxy-5-methyl-2(5H)-furanone 

Downstream Products

• 760-78-1 2-aminopentanoic acid 

Relevant articles and documents

Enantioselective Synthesis of γ-Hydroxynorvaline

A new synthesis of enantiomerically pure γ-hydroxynorvaline is described. The key step involves diastereoselective alkylation of the chiral Schiff base 1 with primary iodo derivatives 2 easily prepared from propylene oxide.

Asymmetric Induction in Acyclic Radical Reactions: Enantioselective Syntheses of α-Amino Acids via Carbon-Carbon Bond Forming Radical Reactions.

The derivative of glycine, 8-phenylmenthyl N-Boc-2-bromoglycinate 1 reacted with allyltri-n-butylstannanes via the corresponding radical 2 by the SH2' mechanism to give (2S) allyl amino acid derivatives with high diastereoselectivity.The reaction of 1 with triphenyl(1,2-propadienyl)stannane and triphenyl(2-propynyl)stannane gave the (2S) allenyl and (2S) propargyl amino acid derivatives respectively also with high diastereoselectivity but by a different mechanism.