72277-16-8

Basic information

• Product Name: ethyl 3-phenylhexanoate
• Synonyms: ethyl 3-phenylhexanoate
• CAS NO: 72277-16-8
• Molecular Weight: 220.312
• Mol File: 72277-16-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: ethyl 3-phenylhexanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-phenylhexanoate(72277-16-8)
• EPA Substance Registry System: ethyl 3-phenylhexanoate(72277-16-8)

Safety Data

• Hazardous Substances Data: 72277-16-8(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 5703-52-6 3-phenylhexanoic acid 
• 27829-72-7 ethyl (E)-hex-2-enoate 
• 591-51-5 phenyllithium 
• 54653-25-7 ethyl hex-5-enoate 
• 143-66-8 sodium tetraphenyl borate 
• 72277-01-1 diethyl 1-trimethylsilyloxy-3-phenyl-2-propenylphosphonate 
• 14371-10-9 (E)-3-phenylpropenal 
• 107-08-4 1-iodo-propane 

Relevant articles and documents

Method To Prepare beta-Functionalized Aliphatic Esters

The invention pertains to a new route to prepare β-functionalized carboxylic acid esters in a one-pot reaction, by reacting an olefinic acid ester in the presence of a catalyst system, comprising a Rh(I)-complex, together with an aryl boron or a diamine a

A METHOD TO PREPARE BETA - FUNCTIONALIZED ALIPHATIC ESTERS

The invention pertains to a new route to prepare β-functionalized carboxylic acid esters in a one-pot reaction, by reacting an olefinic acid ester in the presence of a catalyst system, comprising a Rh(I)-complex, together with an aryl boron or a diamine a

Potassium trifluoro(organo)borates in rhodium-catalyzed 1,4-additions to α,β-unsaturated esters

This letter describes an efficient and enantioselective conjugate addition of highly stable potassium trifluoro(organo)borates to α,β- unsaturated esters. This reaction, catalyzed by chiral rhodium(I) complexes, affords Michael adducts with high yields an