2549-35-1

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Oxazolemethanol, 2,5-diphenylis used as a building block for the synthesis of pharmaceutical compounds. Its unique structure, including the oxazole ring and phenyl groups, allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, 4-Oxazolemethanol, 2,5-diphenylserves as an intermediate in the synthesis of various agrochemicals. Its aromatic nature and potential for molecular interactions make it a valuable component in the creation of effective pesticides and other agricultural chemicals.
Used in Materials Science:
4-Oxazolemethanol, 2,5-diphenylmay be utilized in materials science for the development of novel materials with specific properties. Its aromatic character and structural features could contribute to the design of materials with tailored characteristics for various applications.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 4-Oxazolemethanol, 2,5-diphenylis employed in the preparation of a wide range of organic compounds. Its versatility in chemical reactions allows for the synthesis of diverse molecules with potential applications in various industries.
Further research is essential to fully understand the properties and potential uses of 4-Oxazolemethanol, 2,5-diphenylin these and other fields, as its unique structure and characteristics may offer significant advantages in the development of new products and technologies.

Upstream product

• 92-71-7 2,5-diphenyloxazole 
• 68-12-2 N,N-dimethyl-formamide 
• 71-43-2 benzene 
• 55044-06-9 methyl 2-phenyl-2-oxazoline-4-carboxylate 
• 932-90-1 Benzaldoxime 
• 100-47-0 benzonitrile 
• 100-52-7 benzaldehyde 
• 5333-86-8 ethyl benzimidate hydrochloride 
• 59171-72-1 2-phenyl-oxazole-4-carboxylic acid methyl ester 
• 25755-94-6 methyl 2,5-diphenyloxazole-4-carboxylate 
• 119-51-7 1-phenyl-1,2-propanedione 2-oxime 
• 2549-30-6 4-Methyl-2,5-diphenyloxazole N-oxide 
• 93729-29-4 ethyl 2,5-diphenyloxazole-4-carboxylate 
• 2549-33-9 4-(chloromethyl)-2,5-diphenyloxazole 

Downstream Products

• 337478-96-3 4-hydroxymethyl-2,5-diphenyloxazole acrylate 
• 201033-47-8 4-Azidomethyl-2,5-diphenyl-oxazole 
• 90011-96-4 C-(2,5-Diphenyl-oxazol-4-yl)-methylamine 
• 113923-95-8 2,5-diphenyl-4-vinyloxazole 
• 400625-37-8 3-[4-(2,5-diphenyl-oxazol-4-ylmethoxy)-phenyl]-propan-1-ol 
• 400625-45-8 6-(2,5-diphenyl-oxazol-4-ylmethoxy)-hexanal 
• 400625-41-4 6-(2,5-diphenyl-oxazol-4-ylmethoxy)-hexan-1-ol 
• 132198-58-4 4-formyl-2,5-diphenyloxazole 
• 133130-86-6 4-bromomethyl-2,5-diphenyloxazole 

Relevant academic research and scientific papers

Pd(ii)-catalyzed direct C5-arylation of azole-4-carboxylates through double C-H bond cleavage

The first palladium-catalyzed direct C5-arylation of azole-4-carboxylates with simple unactivated arenes through double C-H bond cleavage is realized. This protocol provided a straightforward access to diverse 5-arylsubstituted azole-4-carboxylic derivatives with good functional group tolerance. The Royal Society of Chemistry 2012.

Synthesis, evaluation and incorporation into liposomes of 4-functionalised-2,5-diphenyloxazole derivatives for application in scintillation proximity assays

The preparation of a series of 4-functionalised-2,5-diphenyloxazoles is described. The scintillating efficiency of each of these 'scintilipid' molecules has been evaluated in the presence of ionising radiation. Each 'scintilipid' has been assessed for the ability to assemble, with other lipids, into liposomes, under a variety of preparative conditions. Each liposomal preparation has been monitored for the ability to scintillate in the presence of ionising radiation. The optimal 'scintilipid', both in terms of effective liposomal formation and scintillation efficiency, has been determined.

Synthesis and scintillating efficiencies of 4-functionalised-2,5-Diphenyloxazoles

A series of 4-functionalised-2,5-diphenyloxazoles has been synthesised. Each member of the series has been assessed for the ability to scintillate in the presence of ionising radiation. The scintillation counting efficiency of each member of the series has been determined relative to 2,5-diphenyloxazole, a widely used scintillant molecule.