84672-13-9

Basic information

• Product Name: 4-(4-methoxyphenyl)-5-methyl-2-phenyloxazole
• Synonyms: 4-(4-methoxyphenyl)-5-methyl-2-phenyloxazole
• CAS NO: 84672-13-9
• Molecular Weight: 265.312
• Mol File: 84672-13-9.mol

Chemical Properties

• CAS DataBase Reference: 4-(4-methoxyphenyl)-5-methyl-2-phenyloxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-methoxyphenyl)-5-methyl-2-phenyloxazole(84672-13-9)
• EPA Substance Registry System: 4-(4-methoxyphenyl)-5-methyl-2-phenyloxazole(84672-13-9)

Safety Data

• Hazardous Substances Data: 84672-13-9(Hazardous Substances Data)

Upstream product

• 55705-15-2 1-(4-methoxyphenyl)-2-(benzoyloxy)propan-1-one 
• 98-88-4 benzoyl chloride 
• 1464-98-8 N-(prop-2-yn-1-yl)benzamide 
• 5221-67-0 5-methyl-2-phenyloxazole 
• 197719-26-9 4-bromo-5-methyl-2-phenyloxazole 
• 75-16-1 methylmagnesium bromide 
• 121-97-1 4-Methoxypropiophenone 
• 21086-33-9 2-bromo-1-(4-methoxyphenyl)-1-propanone 
• 532-32-1 sodium benzoate 

Downstream Products

• 84672-19-5 4-(5-Methyl-2-phenyl-oxazol-4-yl)-phenol 
• 84686-94-2 2-{4-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-phenoxy}-butyric acid ethyl ester 
• 84671-81-8 2-{4-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-phenoxy}-propionic acid ethyl ester 
• 84671-98-7 2-{4-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-phenoxy}-butyric acid 
• 84671-79-4 2-Methyl-2-[4-(5-methyl-2-phenyl-oxazol-4-yl)-phenoxy]-propionic acid ethyl ester 
• 84671-78-3 2-[4-(5-Methyl-2-phenyl-oxazol-4-yl)-phenoxy]-propionic acid ethyl ester 
• 84671-77-2 [4-(5-Methyl-2-phenyl-oxazol-4-yl)-phenoxy]-acetic acid ethyl ester 
• 84671-96-5 2-Methyl-2-[4-(5-methyl-2-phenyl-oxazol-4-yl)-phenoxy]-propionic acid 

Relevant articles and documents

Cyanide-Free Cyanation of sp2 and sp-Carbon Atoms by an Oxazole-Based Masked CN Source Using Flow Microreactors

This work reports a cyanide-free continuous-flow process for cyanation of sp2 and sp carbons to synthesize aryl, vinyl and acetylenic nitriles from (5-methyl-2-phenyloxazol-4-yl) boronic acid [OxBA] reagent as a sole source of carbon-bound mask

Alkynyl Thioethers in Gold-Catalyzed Annulations To Form Oxazoles

Non-oxidative, regioselective, and convergent access to densely functionalized oxazoles is realized in a functional-group tolerant manner using alkynyl thioethers. Sulfur-terminated alkynes provide access to reactivity previously requiring strong donor-substituted alkynes such as ynamides. Sulfur does not act in an analogous donor fashion in this gold-catalyzed reaction, thus leading to complementary regioselective outcomes and addressing the limitations of using ynamides.

Potential Hypolipidemic Agents: Part I-Synthesis and Hypolipidemic Activity of Some 4-(2,5-Substituted oxazole-4-yl)phenoxyalkanoic Acid Derivatives

A series of 4-(2-aryl-5-alkyl-aryloxazol-4-yl)phenoxyalkanoic acid derivatives (VI, 1-32) have been synthesised by O-alkylation of the corresponding 2-aryl-4-(4-hydroxyphenyl)-5-alkyl/aryloxazoles (Va-g) and evaluated for their hypolipidemic activity in rats of Wistar strain.Several compounds in this series show hypolipidemic activity comparable with that of the standard drug clofibrate at 200 mg/kg (p.o) dose.