51039-53-3

Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-5-PHENYL-1,3,4-OXADIAZOLE is used as a pharmaceutical agent for its potential antiviral, antimicrobial, and anticancer properties. Its unique structure allows it to interact with biological targets, making it a promising candidate for the development of new drugs to combat various diseases.
Used in Bioimaging Applications:
In the field of bioimaging, 2-BROMO-5-PHENYL-1,3,4-OXADIAZOLE is utilized as a fluorescence probe. Its optical properties enable it to be used for visualizing and tracking biological processes at the molecular level, providing valuable insights into cellular mechanisms and aiding in the diagnosis and study of diseases.
Used in Organic Chemistry Research:
2-BROMO-5-PHENYL-1,3,4-OXADIAZOLE also serves as a key intermediate in organic synthesis, particularly in the development of new compounds with potential applications in various industries. Its reactivity and structural features make it a versatile building block for creating novel molecules with tailored properties.

InChI:InChI=1S/C8H5BrN2O/c9-8-11-10-7(12-8)6-4-2-1-3-5-6/h1-5H

Upstream product

• 825-56-9 2-phenyl-1,3,4-oxadiazole 
• 613-94-5 benzoic acid hydrazide 
• 65-85-0 benzoic acid 
• 93-89-0 benzoic acid ethyl ester 
• 1612-76-6 2-amino-5-phenyl-1,3,4-oxadiazole 
• 57943-70-1 dibenzoyldiimide 
• 3294-60-8 phenyl(tribromomethyl)mercury(II) 

Downstream Products

• 1225463-77-3 tert-butyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)piperazine-1-carboxylate 
• 1374348-12-5 2-((2-methoxyphenyl)ethynyl)-5-phenyl-1,3,4-oxadiazole 
• 1374348-14-7 2-(non-1-ynyl)-5-phenyl-1,3,4-oxadiazole 
• 1374348-11-4 2-phenyl-5-(thiophen-2-ylethynyl)-1,3,4-oxadiazole 
• 1374348-13-6 2-(naphthalen-2-ylethynyl)-5-phenyl-1,3,4-oxadiazole 

Relevant academic research and scientific papers

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present specification provides a compound represented by chemical formula 1 and an organic light emitting device including the same. The compound may improve lifespan characteristics of the organic light emitting device.

MONITORING AND DOSAGE CONTROL OF TAGGED TREATMENT POLYMERS IN INDUSTRIAL WATER SYSTEMS

The present invention relates to a fluorescently-tagged (co)polymer useful as a scale inhibitor in industrial water systems. Said (co)polymer comprises a (i) reactive fluorescent compound selected from a diazole compound (ii) at least one monoethylenicall

TAGGED TREATMENT POLYMERS FOR MONITORING ANTISCALANT CONCENTRATIONS IN INDUSTRIAL WATER SYSTEMS

The present invention relates to a fluorescently-tagged (co)polymer useful as a scale inhibitor in industrial water systems. Said (co)polymer comprises a (i) reactive fluorescent compound selected from a diazole compound (ii) at least one monoethylenicall

Synthesis and evaluation of in vivo anticonvulsant activity of 2,5-disubstituted-1,3,4-oxadiazole derivatives

A series of new 2,5-disubstituted-1,3,4-oxadiazole derivatives 8(a-o) was synthesized by the reaction of 1-(5-phenyl-1,3,4-oxadiazol-2-yl)piperazine with various sulfonyl chlorides. The synthesized compounds were characterized by elemental analyses,

General facile synthesis of 2,5-diarylheteropentalenes

Palladium-catalyzed cross-coupling reactions of various heteropentalene derivatives were systematically studied. A general three-step synthesis of 2,5-diarylheteropentalenes involving two Suzuki or Negishi couplings and a regiospecific bromination was developed. Nonsymmetrical 2,5-diaryl-furans, thiophenes, pyrroles, 1,3-thiazoles, 1,3-oxazoles, 1,3,4-thiadiazoles, and 1,3,4-oxadiazoles were prepared in 31-67% isolated yield (three steps).