25433-30-1

Basic information

• Product Name: 2-phenyl-5-(2-pyridyl)-1,3,4-oxadiazole
• Synonyms: 2-phenyl-5-(2-pyridyl)-1,3,4-oxadiazole;"2-phenyl-5-(2-pyridyl)-1,3,4-oxadiazole (pop);2-phenyl-5-(pyridin-2-yl)-1,3,4-oxadiazole
• CAS NO: 25433-30-1
• Molecular Formula: C₁₃H₉N₃O
• Molecular Weight: 223.23006
• Mol File: 25433-30-1.mol
• Article Data: 18

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-phenyl-5-(2-pyridyl)-1,3,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-5-(2-pyridyl)-1,3,4-oxadiazole(25433-30-1)
• EPA Substance Registry System: 2-phenyl-5-(2-pyridyl)-1,3,4-oxadiazole(25433-30-1)

Safety Data

• Hazardous Substances Data: 25433-30-1(Hazardous Substances Data)

Upstream product

• 98-07-7 Benzotrichlorid 
• 1215-54-9 Benzoic acid N'-pyridin-2-ylmethyl-hydrazide 
• 33893-89-9 5-(2-pyridyl)-1H-tetrazole 
• 98-88-4 benzoyl chloride 
• 98-98-6 2-Picolinic acid 
• 18039-42-4 5-Phenyl-1H-tetrazole 
• 109-06-8 α-picoline 
• 613-94-5 benzoic acid hydrazide 
• 93-58-3 benzoic acid methyl ester 
• 65-85-0 benzoic acid 
• 1121-60-4 pyridine-2-carbaldehyde 
• 33893-89-9 2-(2H-tetrazol-5-yl)-pyridine 
• 93-97-0 benzoic acid anhydride 
• 54571-23-2 pyridine-2-carboxylic acid N'-benzoyl-hydrazide 

Downstream Products

• 1245722-53-5 [Cu(bis[2-(diphenylphosphino)phenyl]-ether)2(2-phenyl-5-(pyridin-2-yl)-1,3,4-oxadiazole)]BF₄ 
• 1245722-49-9 [Cu(triphenylphosphine)2(2-phenyl-5-(pyridin-2-yl)-1,3,4-oxadiazole)]BF₄ 

Relevant articles and documents

A rhenium complex doped in a silica molecular sieve for molecular oxygen sensing: Construction and characterization

This paper reported a diamine ligand and its Re(I) complex for potential application in oxygen sensing. The novelty of this diamine ligand localized at its increased conjugation chain which had a typical electron-withdrawing group of 1,3,4-oxadiazole. Ele

Facile synthesis of 1,3,4-oxadiazoles via iodine promoted oxidative annulation of methyl-azaheteroarenes and hydrazides

An oxidative sp3 C–H bond of methyl-azaheteroarenes protocol was reported for the synthesis of 1,3,4-oxadiazoles via [4 + 1] annulation with hydrazides. This protocol enables 1,3,4-oxadiazole and quinoline linked diheterocycles via selective oxidation of sp3 C–H bond of methyl-azaheteroarenes in the presence of I2-DMSO. The reaction has a broad substrate scope and good functional group tolerance for methyl-azaheteroarenes and hydrazides.

Preparation and acetylcholinesterase inhibitory activities of pyridine-based 1,3,4-oxadiazole derivatives

Fourteen pyridine-based 1,3,4-oxadiazole derivatives were synthesized from pyridine-2-carboxaldehyde via iodine-mediated oxidative cyclisation with substituted hydrazide by using the impregnation method. Their structures were confirmed by melting point,