58653-96-6

Basic information

• Product Name: Propanoic acid, 2-(benzoyloxy)-, methyl ester
• CAS NO: 58653-96-6
• Molecular Formula: C11H12O4
• Molecular Weight: 208.214
• Mol File: 58653-96-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 2-(benzoyloxy)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2-(benzoyloxy)-, methyl ester(58653-96-6)
• EPA Substance Registry System: Propanoic acid, 2-(benzoyloxy)-, methyl ester(58653-96-6)

Safety Data

• Hazardous Substances Data: 58653-96-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 769-78-8 vinyl benzoate 
• 78626-51-4 methyl 2-(benzoyloxy)-2-propenoate 
• 186581-53-3 diazomethane 
• 52210-17-0 Benzoic acid (E)-(R)-1-methyl-3-(2,2,6-trimethyl-4-oxo-cyclohexyl)-allyl ester 
• 17392-83-5 (R)-Methyl lactate 
• 98-88-4 benzoyl chloride 
• 547-64-8 methyl lactate 

Relevant articles and documents

Tuning of the structures of chiral phosphane-phosphites: Application to the highly enantioselective synthesis of α-acyloxy phosphonates by catalytic hydrogenation

A family of new chiral phosphane-phosphites 5 has been prepared and employed in the synthesis of rhodium complexes of formulation [Rh(cod)(5)]BF4 (7). The use of bulky phosphane or phosphite groups in the preparation of 7 avoids the formation of undesired

Hydroesterification of Olefins Catalyzed by Pd(OAc)2 Immobilized on Montmorillonite

Palladium acetate immobilized on montmorillonite is an efficient catalyst for the hydroesterification of olefins with carbon monoxide and methanol, in the presence of triphenylphosphine and an acid promoter, affording branched chain esters.The reaction is regiospecific for aryl olefins as well as for vinyl benzoate and regioselective for aliphatic olefins.