52955-65-4

Basic information

• Product Name: (5-methyl-2-phenyloxazol-4-yl)(phenyl)methanone
• Synonyms: (5-methyl-2-phenyloxazol-4-yl)(phenyl)methanone
• CAS NO: 52955-65-4
• Molecular Weight: 263.296
• Mol File: 52955-65-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (5-methyl-2-phenyloxazol-4-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-methyl-2-phenyloxazol-4-yl)(phenyl)methanone(52955-65-4)
• EPA Substance Registry System: (5-methyl-2-phenyloxazol-4-yl)(phenyl)methanone(52955-65-4)

Safety Data

• Hazardous Substances Data: 52955-65-4(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 93-91-4 1-phenylbutan-1,3-dione 
• 18735-74-5 5-methyl-2-phenyloxazole-4-carboxylic acid 
• 2009-96-3 2-diazo-1-phenylbutane-1,3-dione 
• 14677-93-1 3-phenyl-4-benzoyl-5-methylisoxazole 
• 51655-71-1 2-phenyl-5-methyl-4-oxazolecarboxylic acid chloride 
• 71-43-2 benzene 
• 42812-93-1 1-(3,5-diphenylisoxazol-4-yl)ethan-1-one 
• 16002-63-4 phenylmagnesium iodide 
• 2940-19-4 4-acetyl-5-methyl-2-phenyloxazole 

Downstream Products

• 57742-59-3 1-(5-methyl-2-phenyl-oxazol-4-yl)-1-phenyl-ethanol 

Relevant articles and documents

Electrochemically promoted synthesis of polysubstituted oxazoles from β-diketone derivatives and benzylamines under mild conditions

An efficient electrochemical synthesis of poly-substituted oxazoles from readily available β-diketone derivatives and benzylamines is described. This electrochemical procedure does not need hazardous oxidants and transition metal catalysts as well as molecular I2 additives. Compared with the traditional thermo-chemical method, the present electrochemical method is greener and more efficient. The Royal Society of Chemistry 2014.

Photochemistry of 4-Acylisoxazoles

The photochemistry of 4-acylisoxazoles 4, 5, 13, 14, and 17 was investigated in an effort to clarify literature contradictions and anomalies and to provide a more detailed picture of the nature and number of intermediates involved in photoreactions of these systems.In contrast to a previous report on the photorearrangement of 14, both oxazoles expected from a 2H-azirine intermediate have been observed.Wavelength studies of 5 and the derived 2H-azirine 10 revealed evidence for the involvement of at least two distinct product-forming intermediates.The results of quantum yield and laser photolysis measurements for ketones 4, 14, and 17 have been interpreted in terms of rapid openings of triplet states to form diradical-like intermediates coupled with efficient reclosures (70-99percent).