476187-10-7

Basic information

• Product Name: (Z)-3-((S)-2-Hydroxy-1-phenyl-ethylamino)-but-2-enoic acid methyl ester
• CAS NO: 476187-10-7
• Molecular Weight: 235.283
• Mol File: 476187-10-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (Z)-3-((S)-2-Hydroxy-1-phenyl-ethylamino)-but-2-enoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-3-((S)-2-Hydroxy-1-phenyl-ethylamino)-but-2-enoic acid methyl ester(476187-10-7)
• EPA Substance Registry System: (Z)-3-((S)-2-Hydroxy-1-phenyl-ethylamino)-but-2-enoic acid methyl ester(476187-10-7)

Safety Data

• Hazardous Substances Data: 476187-10-7(Hazardous Substances Data)

Upstream product

• 20989-17-7 (2S)-2-phenylglycinol 
• 105-45-3 acetoacetic acid methyl ester 

Downstream Products

• 454451-67-3 (3S)-(8S)-(8aR)-methyl-5-oxo-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-8-carboxylic acid methyl ester 
• 454451-70-8 (3S)-(8R)-(8aR)-methyl-5-oxo-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-8-carboxylic acid methyl ester 
• 595582-07-3 1-(2-hydroxy-(1S)-phenyl-ethyl)-2-methyl-6-oxo-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid methyl ester 

Relevant articles and documents

Synthesis of enantiopure cis- and trans-2,3-disubstituted piperidines

The synthesis of enantiopure cis- and trans-2,3-disubstituted piperidines 4 is described. The key step of the synthesis involves the stereoselective reduction of chiral nonracemic lactams 2 by using BH3·Me2S. A rationalization of the stereoselectivity is presented.