1351766-64-7

Basic information

• Product Name: (R)-3-ethoxy-3-oxo-1-phenylpropyl decanoate
• Synonyms: (R)-3-ethoxy-3-oxo-1-phenylpropyl decanoate
• CAS NO: 1351766-64-7
• Molecular Weight: 348.483
• Mol File: 1351766-64-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-3-ethoxy-3-oxo-1-phenylpropyl decanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-ethoxy-3-oxo-1-phenylpropyl decanoate(1351766-64-7)
• EPA Substance Registry System: (R)-3-ethoxy-3-oxo-1-phenylpropyl decanoate(1351766-64-7)

Safety Data

• Hazardous Substances Data: 1351766-64-7(Hazardous Substances Data)

Upstream product

• 5764-85-2 Ethyl 3-hydroxy-3-phenylpropanoate 
• 112-13-0 n-decanoyl chloride 
• 4704-31-8 vinyl caprate 
• 30673-36-0 n-butyl decanoate 
• 2311-59-3 isopropyl decanoate 
• 110-38-3 decanoic acid ethyl ester 
• 334-48-5 1-decanoic acid 
• 1351766-79-4 3-ethoxy-3-oxo-1-phenylpropyl decanoate 

Downstream Products

• 72656-47-4 ethyl (R)-3-hydroxy-3-phenylpropanoate 

Relevant articles and documents

Lipase mediated sequential resolution of aromatic β-hydroxy esters using fatty acid derivatives

The lipase-catalyzed kinetic resolution of a series of aromatic β-hydroxy esters in organic media has been investigated. Decanoic acid and its esters were successfully used as acyl donors for selective O-acylation. The regio- and enantioselective enzymatic hydrolysis of the decanoate moiety of the diesters was also investigated. The effects of water, reaction temperature, and solvent type, and also the influence of substrates structure on the catalytic behavior of potential commercially available lipases were studied. A novel procedure was developed for the efficient and highly stereoselective synthesis of both enantiomers of both novel and known target compounds. Copyright