37009-57-7

Basic information

• Product Name: Oxazole, 5-(4-methylphenyl)-2-phenyl-
• Synonyms: Oxazole,5-(4-methylphenyl)-2-phenyl;5-(4-methylphenyl)-2-phenyloxazole;2-phenyl-5-(4-methylphenyl)-oxazole;2-phenyl-5-p-tolyloxazole;5-(p-methylphenyl)-2-phenyloxazole
• CAS NO: 37009-57-7
• Molecular Formula: C16H13NO
• Molecular Weight: 235.285
• Mol File: 37009-57-7.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Oxazole, 5-(4-methylphenyl)-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 5-(4-methylphenyl)-2-phenyl-(37009-57-7)
• EPA Substance Registry System: Oxazole, 5-(4-methylphenyl)-2-phenyl-(37009-57-7)

Safety Data

• Hazardous Substances Data: 37009-57-7(Hazardous Substances Data)

Upstream product

• 619-41-0 4-(bromoacetyl)toluene 
• 100-46-9 benzylamine 
• 766-97-2 4-n-methylphenylacetylene 
• 5301-96-2 4-(p-tolyl)-1H-[1,2,3]triazole 
• 2835-06-5 phenylglycin 
• 4224-96-8 3-phenyl-1-p-tolylprop-2-en-1-one 
• 61650-22-4 N-(pivaloyloxy)benzamide 
• 108-90-7 chlorobenzene 
• 143659-19-2 5-(4-methylphenyl)-1,3-oxazole 
• 3240-11-7 Phenylacetylene-d1 
• 582-61-6 benzoyl azide 
• 1004651-40-4 (E)-1-(4-methylphenyl)-3-{(4-(trifluoromethyl)phenyl)}-2-propen-1-one 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 104-09-6 4-methylphenylacetaldehyde 

Downstream Products

• 2681-23-4 4-(2-phenyl-oxazol-5-yl)-benzaldehyde 
• 4829-87-2 triphenyl-[4-(2-phenyl-oxazol-5-yl)-benzyl]-phosphonium; bromide 

Relevant articles and documents

Access to (Z)-β-Substituted Enamides from N1-H-1,2,3-Triazoles

A direct ring-opening/nucleophilic substitution reaction of N1-H-1,2,3-triazoles has been described. Divergent (Z)-β-halogen- or sulfonyl-substituted enamides could be stereospecifically synthesized in a tunable manner. This strategy might not only enable

Divergent Conversion of N-Acyl-isoxazol-5(2 H)-ones to Oxazoles and 1,3-Oxazin-6-ones Using Photoredox Catalysis

The fragmentation of N-acyl-isoxazol-5-ones using visible light photoredox catalysis has been disclosed. The catalyst-controlled divergent mechanisms, namely the oxidative and reductive quenching catalytic cycle, are utilized. Various oxazoles and 1,3-oxazin-6-ones are selectively obtained from the same isoxazol-5-one skeleton under mild conditions.

Metal-free iodine(iii)-promoted synthesis of 2,5-diaryloxazoles

A nonmetal-catalyzed oxidative cyclization to achieve 2,5-disubstituted oxazoles from inexpensive and readily available substituted chalcone, (diacetoxyiodo)benzene (PIDA) and ammonium acetate (NH4OAc) at room temperature is described. The reaction forms a variety of 2,5-diaryloxazoles in good to excellent yields with broad substrate scope under mild conditions without the requirement of ligands and additional bases.