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Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
4-Bromo-2-phenyl oxazole serves as a key building block in the creation of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of compounds with specific biological activities, contributing to the advancement of new drugs and agricultural products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Bromo-2-phenyl oxazole is utilized for its potential to form biologically active compounds. Its reactivity and structural features make it a valuable component in the design and synthesis of new molecules with therapeutic properties.
Used in the Development of Novel Materials:
4-Bromo-2-phenyl oxazole also finds application in the development of innovative materials. Its unique chemical properties enable the creation of new substances with specific characteristics, broadening the scope of material science and technology.
Used as a Reagent in Organic Synthesis:
Furthermore, 4-Bromo-2-phenyl oxazole is employed as a reagent in organic synthesis processes. Its ability to participate in various chemical reactions makes it a versatile tool for the production of a wide range of chemical compounds.

Upstream product

• 92629-11-3 5-bromo-2-phenyl-1,3-oxazole 
• 7127-19-7 2-phenyl-1,3-oxazoline 

Downstream Products

• 1092073-99-8 2-methylsulfanyl-4-(2-phenoxazol-4-yl)pyrimidine 
• 838-41-5 2,4-diphenyl-1,3-oxazole 
• 1092073-97-6 2-fluoro-4-(2-phenyloxazol-4-yl)pyridine 
• 197719-26-9 4-bromo-5-methyl-2-phenyloxazole 

Relevant academic research and scientific papers

First halogen dance reaction on oxazoles. Synthesis of 4,5-disubstituted 2-phenyloxazoles

The halogen dance reaction was investigated on the oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology. Georg Thieme Verlag Stuttgart.

Composite tetraheteroarylenes and related higher cyclic oligomers of heteroarenes produced by palladium-catalyzed direct coupling

Substantial research interests have been focused on cyclic π-conjugated molecules owing to their unique chemical and physical properties. By constructing hybrid aromatic arrays within these cyclic systems, new series of composite macrocycles would be prov

A comparative study on stille cross-coupling reactions of 2-phenylthiazoles and 2-phenyloxazoles

A systematic study of the cross-coupling capability of the 4- and 5-positions of 2-phenylthiazoles and -oxazoles under Stille conditions is presented. The azoles were both applied as stannanes and as the halide component. The obtained results were compared regarding the position of the halide and Bu3Sn group. In order to establish a general reactivity platform for those heterocyclic systems, a broad variety of aromatic and heteroaromatic halides were coupled and some significant differences concerning the coupling properties of the investigated systems were observed. Georg Thieme Verlag Stuttgart.