14367-05-6

Basic information

• Product Name: threo-2-ethyl 3-hydroxy 3-phenylpropanoic methyl ester
• CAS NO: 14367-05-6
• Molecular Weight: 208.257
• Mol File: 14367-05-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: threo-2-ethyl 3-hydroxy 3-phenylpropanoic methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: threo-2-ethyl 3-hydroxy 3-phenylpropanoic methyl ester(14367-05-6)
• EPA Substance Registry System: threo-2-ethyl 3-hydroxy 3-phenylpropanoic methyl ester(14367-05-6)

Safety Data

• Hazardous Substances Data: 14367-05-6(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 14367-04-5 erythro-2-Ethyl-3-hydroxy-3-phenylpropionsaeure 
• 5336-76-5 methyl 2-benzoylbutanoate 
• 623-42-7 butanoic acid methyl ester 
• 100-52-7 benzaldehyde 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 3196-15-4 Methyl 2-bromobutyrate 
• 55453-12-8 (1-methoxybut-1-enyloxy)trimethylsilane 
• 79868-63-6 2-(α-hydroxy-benzyl)-butyric acid methyl ester 
• 623-43-8 methyl crotonate 
• 14367-04-5 threo-2-Ethyl-3-hydroxy-3-phenylpropionsaeure 

Relevant articles and documents

Reductive aldol-type reaction of α,β-unsaturated esters with aldehydes or ketones in the presence of Rh catalyst and Et2Zn

The reaction of RhCl(PPh3)3 with Et2Zn easily generated a rhodium-hydride complex (Rh-H) that added to α,β-unsaturated esters to form rhodium enolate complexes by formal 1,4-reduction. These rhodium enolates gave the corre

Chromium(II)-Mediated Reformatsky Reactions of Carboxylic Esters with Aldehydes

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Design of α-Alkyl β-Hydroxy Esters Suitable for Providing Optical Resolution by Lipase Hydrolysis

A study of the lipase-catalyzed hydrolyses of various α-substituted β-acetoxy esters revealed that a sulfur functional group in the ester, which could play an important role in the stereorecognition by lipase A6 (Aspergillus sp.) and an anti conformation