126400-92-8

Basic information

• Product Name: ethyl (3S)-3-{[(benzyloxy)carbonyl]amino}butanoate
• Synonyms: ethyl (3S)-3-{[(benzyloxy)carbonyl]amino}butanoate
• CAS NO: 126400-92-8
• Molecular Weight: 265.309
• Mol File: 126400-92-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl (3S)-3-{[(benzyloxy)carbonyl]amino}butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (3S)-3-{[(benzyloxy)carbonyl]amino}butanoate(126400-92-8)
• EPA Substance Registry System: ethyl (3S)-3-{[(benzyloxy)carbonyl]amino}butanoate(126400-92-8)

Safety Data

• Hazardous Substances Data: 126400-92-8(Hazardous Substances Data)

Upstream product

• 5303-65-1 3-aminobutanoic acid ethyl ester 
• 922705-30-4 phenylmethyl (4S)-4-methyl-6-oxo-1,3-oxazinane-3-carboxylate 
• 64-17-5 ethanol 
• 426254-23-1 (-)-tert-butyl (S)-N-(benzyloxycarbonyl)-3-aminobutanoate 
• 100-46-9 benzylamine 
• 501-53-1 benzyl chloroformate 
• 5303-65-1 (S)-ethyl 3-aminobutyrate 

Downstream Products

• 685544-49-4 (R)-3-{[2-(4-cyanophenyl)-1-oxo-2,8-diazaspiro[4.5]decane-8-carbonyl]amino}butyric acid ethyl ester 
• 685544-48-3 3-(4-nitrophenoxycarbonylamino)butyric acid ethyl ester 
• 5303-65-1 ethyl 3-(R)-methyl-β-alanine 
• 83509-88-0 (S)-3-benzyloxycarbonylaminobutyric acid 
• 99029-37-5 ethyl (3S)-3-(N-benzyloxycarbonyl-N-ethylamino)butyrate 
• 99029-39-7 ethyl (3R)-3-(N-benzyloxycarbonyl-N-ethylamino)butyrate 

Relevant articles and documents

Diastereoselective synthesis of α-methyl and α-hydroxy-β- amino acids via 4-substituted-1,3-oxazinan-6-ones

(Chemical Equation Presented) 1,3-Oxazinan-6-ones have been utilized in a series of enolate reactions to produce 5-hydroxy and 5-alkyl-4-substituted-1,3- oxazinan-6-ones with excellent trans diastereoselectivity. Highlighting the versatility of the oxazin

Candida antarctica lipase catalyzed resolution of ethyl (±)-3-aminobutyrate

Candida antarctica lipase efficiently catalyzes acetylation and hydrolysis of ethyl (±)-3-aminobutyrate.