116897-05-3

Basic information

• Product Name: Oxazole, 2-(4-methylphenyl)-4-phenyl-
• CAS NO: 116897-05-3
• Molecular Formula: C16H13NO
• Molecular Weight: 235.285
• Mol File: 116897-05-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Oxazole, 2-(4-methylphenyl)-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 2-(4-methylphenyl)-4-phenyl-(116897-05-3)
• EPA Substance Registry System: Oxazole, 2-(4-methylphenyl)-4-phenyl-(116897-05-3)

Safety Data

• Hazardous Substances Data: 116897-05-3(Hazardous Substances Data)

Upstream product

• 54797-44-3 2-oxo-2-phenylethyl 4-methylbenzoate 
• 445470-08-6 2-chloro-4-phenyloxazole 
• 5720-05-8 4-methylphenylboronic acid 
• 20662-89-9 4-phenyl-1,3-oxazole 
• 99-94-5 p-Toluic acid 
• 98-80-6 phenylboronic acid 
• 104-85-8 para-methylbenzonitrile 
• 29941-22-8 Bu₂Sn{OCO(4-MeC₆H₄)}2 
• 536-74-3 phenylacetylene 
• 60-12-8 2-phenylethanol 

Downstream Products

• 94-08-6 4-methylbenzoic acid ethyl ester 
• 93-89-0 benzoic acid ethyl ester 
• 99-94-5 p-Toluic acid 
• 65-85-0 benzoic acid 

Relevant articles and documents

METHOD FOR PRODUCING IODOOXAZOLE COMPOUND, AND METHOD FOR PRODUCING OXAZOLE COMPOUND

PROBLEM TO BE SOLVED: To produce an iodooxazole compound inexpensively and safely without using oxidizing agents. SOLUTION: On the basis of the following chemical formula (1) an iminoether compound and an iodinating agent are mixed and reacted with each other with light irradiation, to produce an iodooxazole compound. In the formula (1), R1, R2 each denote an aromatic group. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Divergent Palladium-Catalyzed Tandem Reaction of Cyanomethyl Benzoates with Arylboronic Acids: Synthesis of Oxazoles and Isocoumarins

A palladium-catalyzed tandem reaction of cyanomethyl benzoates with arylboronic acids has been achieved. Substitution at the 2-position of cyanomethyl benzoates was found to be crucial for the selective synthesis of oxazoles and isocoumarins. Cyanomethyl

An iron and copper system catalyzed C-H arylation of azoles with arylboronic acids

An efficient, environmentally friendly, and economical new method for arylation reactions of azoles with arylboronic acids via copper-iron-catalyzed C-H and C-B bond activation has been developed. The protocol tolerates a series of functional groups, such as methoxy, nitro, cyano, chloro, and trifluoromethyl groups.