23012-31-9

Basic information

• Product Name: Oxazole, 2,4-dimethyl-5-phenyl-
• CAS NO: 23012-31-9
• Molecular Formula: C11H11NO
• Molecular Weight: 173.214
• Mol File: 23012-31-9.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Oxazole, 2,4-dimethyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 2,4-dimethyl-5-phenyl-(23012-31-9)
• EPA Substance Registry System: Oxazole, 2,4-dimethyl-5-phenyl-(23012-31-9)

Safety Data

• Hazardous Substances Data: 23012-31-9(Hazardous Substances Data)

Upstream product

• 93-55-0 1-phenyl-propan-1-one 
• 75-05-8 acetonitrile 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 66323-99-7 trimethyl[(Z)-(1-phenyl-1-propenyl)oxy]silane 
• 18793-46-9 (E)-N-(1-Methyl-2-phenylethenyl)ethanamide 
• 18793-46-9 (Z)-N-(1-Methyl-2phenylethenyl)ethanamide 
• 6627-80-1 N-[1-(4-nitro-benzoyl)-vinyl]-acetamide 
• 3123-13-5 N-[1-hydroxymethyl-2-(4-nitro-phenyl)-2-oxo-ethyl]-acetamide 
• 23000-11-5 2,4-dimethyl-5-(4-nitro-phenyl)-oxazole 
• 35947-99-0 2-azido-1-phenyl-1-propanone 
• 81703-28-8 N-<(1R,2S)-(-)-norephedrine>methylamide 
• 492-41-1 (1R,2S)-norephedrine 
• 10026-13-8 phosphorus pentachloride 
• 16735-28-7 N-(1-methyl-2-oxo-2-phenylethyl)acetamide 

Downstream Products

• 76346-93-5 1-(5-Phenyl-4-methyl-2-oxazolyl)octan-2-ol 
• 76346-94-6 2-Isobutyl-4-phenyl-5-methyloxazole 

Relevant articles and documents

Contrasting C- and O-Atom Reactivities of Neutral Ketone and Enolate Forms of 3-Sulfonyloxyimino-2-methyl-1-phenyl-1-butanones

The mechanisms of intramolecular cyclization of 3-sulfonyloxyimino-2-methyl-1-phenyl-1-butanones (1) under basic (DABCO and t-BuOK) and acidic (AcOH and TFA) conditions were investigated by means of experimental and computational methods. The ketone, enol

Umpolung Strategy for Synthesis of β-Ketonitriles through Hypervalent Iodine-Promoted Cyanation of Silyl Enol Ethers

An efficient method to synthesize β-ketonitriles from silyl enol ethers by an umploung hypervalent iodine(III)-CN species generated in situ from PhIO/BF3·Et2O/TMSCN has been developed for the first time. This method can be applied to structurally diverse aromatic and aliphatic substrates and further extended to preparation of bioactive compounds like 5-aminopyrazole and 5-aminoisoxazole.

Synthesis of oxazoles from enamides via phenyliodine diacetate-mediated intramolecular oxidative cyclization

A group of functionalized oxazoles were synthesized in moderate to good yields from enamides via phenyliodine diacetate (PIDA)-mediated intramolecular cyclization. The main advantageous features of the present method include its broad substrate scope and the heavy-metal-free characteristic of the oxidative carbon-oxygen bond formation process.