910547-95-4

Basic information

• Product Name: 4-Oxazolecarboxylic acid, 4,5-dihydro-4-methyl-5-oxo-2-phenyl-, 1-methylethyl ester
• Synonyms: 4-Oxazolecarboxylic acid, 4,5-dihydro-4-methyl-5-oxo-2-phenyl-, 1-methylethyl ester
• CAS NO: 910547-95-4
• Molecular Formula: C14H15NO4
• Molecular Weight: 261.2732
• Mol File: 910547-95-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Oxazolecarboxylic acid, 4,5-dihydro-4-methyl-5-oxo-2-phenyl-, 1-methylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Oxazolecarboxylic acid, 4,5-dihydro-4-methyl-5-oxo-2-phenyl-, 1-methylethyl ester(910547-95-4)
• EPA Substance Registry System: 4-Oxazolecarboxylic acid, 4,5-dihydro-4-methyl-5-oxo-2-phenyl-, 1-methylethyl ester(910547-95-4)

Safety Data

• Hazardous Substances Data: 910547-95-4(Hazardous Substances Data)

Upstream product

• 886466-23-5 4-methyl-5-oxo-2-phenyl-4,5-dihydrooxazole-4-carboxylic acid propyl ester 
• 109-86-4 2-methoxy-ethanol 

Relevant articles and documents

Metal complexes-catalyzed hydrolysis and alcoholysis of organic substrates and their application to kinetic resolution

Metal complexes-catalyzed hydrolysis and alcoholysis of organic substrates such as alkenyl esters, alkenyl ethers, and azlactones (oxazol-5(4H)-ones) are described. These reactions were applied for kinetic resolution of chiral compounds and high selectivities were achieved with vinyl ethers of 2-substituted cyclohexanols, 1,1′-bi-2-naphthols, 1,1′-bi-2-phenols, and 4,4-disubstituted azlactones. Oxidative carbon-carbon bond cleavage reactions, which were found in the course of the study of asymmetric hydrolysis were also described.