94138-70-2

Basic information

• Product Name: 2-(2-benzofuryl)-5-phenyl-1,3,4-oxadiazole
• Synonyms: 2-(2-benzofuryl)-5-phenyl-1,3,4-oxadiazole;2-(2-Benzofuranyl)-5-phenyl-1,3,4-oxadiazole
• CAS NO: 94138-70-2
• Molecular Formula: C₁₆H₁₀N₂O₂
• Molecular Weight: 262.2628
• EINECS: 302-986-0
• Mol File: 94138-70-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-benzofuryl)-5-phenyl-1,3,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-benzofuryl)-5-phenyl-1,3,4-oxadiazole(94138-70-2)
• EPA Substance Registry System: 2-(2-benzofuryl)-5-phenyl-1,3,4-oxadiazole(94138-70-2)

Safety Data

• Hazardous Substances Data: 94138-70-2(Hazardous Substances Data)

Usage

General Description

2-(2-Benzofuryl)-5-phenyl-1,3,4-oxadiazole is a chemical compound with the molecular formula C15H9N3O and a molecular weight of 247.25 g/mol. It is a heterocyclic compound with a five-membered ring structure containing nitrogen and oxygen atoms. 2-(2-Benzofuryl)-5-phenyl-1,3,4-oxadiazole has been studied for its potential applications in organic electronic devices and light-emitting diodes due to its favorable electronic and optical properties. It exhibits strong fluorescence and has been investigated for its potential as a fluorescent probe in biological imaging. Additionally, it has shown promise as a potential antitumor agent due to its ability to inhibit cancer cell growth. 2-(2-Benzofuryl)-5-phenyl-1,3,4-oxadiazole represents an interesting area of research in the field of organic chemistry and has potential applications in various industries.

Upstream product

• 825-56-9 2-phenyl-1,3,4-oxadiazole 
• 91703-34-3 2-(β,β-dibromovinyl)phenol 
• 42974-19-6 benzo[b]furan-2-carbohydrazide 
• 65-85-0 benzoic acid 

Relevant articles and documents

Highly efficient copper/palladium-catalyzed tandem Ullman reaction/arylation of azoles via C-H activation: Synthesis of benzofuranyl and indolyl azoles from 2-(gem-dibromovinyl)phenols(anilines) with azoles

In this paper, a novel and highly efficient copper/palladium-catalyzed tandem intramolecular Ullman-type C-O(N) coupling reaction of 2-(gem-dibromovinyl)phenols(anilines) followed by an intermolecular arylation of azoles through C-H activation has been developed. In the presence of CuBr with Pd(PPh3)2Cl2 used as co-catalyst, and LiO tBu as a base, the one-pot reactions of 2-(gem-dibromovinyl)phenols and 2-(gem-dibromovinyl)anilines with a variety of azoles, including oxazoles, imidazoles, thiazoles, and oxadiazoles underwent smoothly in toluene at 100 °C to generate the corresponding biheteroaryl products in high yields. A tentative mechanism of copper/palladium-catalyzed tandem reaction was described.

Utilization of 2-benzo[b]furan carboxylic acid hydrazide in the synthesis of 1,3,4-oxadiazole derivatives

(Chemical Equation Presented) In this study, the synthesis of series of 2-benzo[b]furan-substituted 1,3,4-oxadiazole derivatives using readily available 2-benzo[b]furan carboxylic acid hydrazide as starting material has been investigated.