1617-94-3

Basic information

• Product Name: N-phenyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-amine
• Synonyms: 1,3,4-oxadiazol-2-amine, N-phenyl-5-(4-pyridinyl)-; N-Phenyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-amine
• CAS NO: 1617-94-3
• Molecular Formula: C₁₃H₁₀N₄O
• Molecular Weight: 238.2447
• Mol File: 1617-94-3.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 430°C at 760 mmHg
• Flash Point: 213.8°C
• Density: 1.3g/cm³
• Vapor Pressure: 1.35E-07mmHg at 25°C
• Refractive Index: 1.649
• CAS DataBase Reference: N-phenyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-amine(1617-94-3)
• EPA Substance Registry System: N-phenyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-amine(1617-94-3)

Safety Data

• Hazardous Substances Data: 1617-94-3(Hazardous Substances Data)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 6954-50-3 1-isonicotinoyl-4-phenylthiosemicarbazide 
• 18440-58-9 1-(N-phenylhydrazono)-1-chloropropanone 
• 54-85-3 isoniazid 
• 4426-68-0 phenyl isoselenocyanate 
• 14389-12-9 5-(4-pyridyl)tetrazole 
• 103-71-9 phenyl isocyanate 
• 55-22-1 pyridine-4-carboxylic acid 
• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 15152-50-8 1-isonicotinoyl-4-phenyl-3-semicarbazide 
• 5285-87-0 phenyl thiocyanate 

Relevant articles and documents

Novel 1,3,4-oxadiazole motifs bearing a quinoline nucleus: Synthesis, characterization and biological evaluation of their antimicrobial, antitubercular, antimalarial and cytotoxic activities

A series of quinoline based 1,3,4-oxadiazole derivatives (8a-l) were synthesized by a chloro-amine coupling reaction approach with different catalysts and solvents. Substituted 1,3,4-oxadiazole intermediates 7a-c were obtained from 2-substituted-N-phenylh

Cyclodesulfurization of Substituted Thiosemicarbazides into 1,3,4-Oxadiazoles via Hydrazonoyl Chlorides

The reaction of thiosemicarbazides 1a-h with hydrazonoyl chlorides 2a-g at ambient temperature, in the presence of triethylamine yielded, in each case, two products. The structure of these compounds was confirmed as 1,3,4-oxadiazoles 14a-h and hydrazonoth

Electrochemically initiated oxidative cyclization: A versatile route for the synthesis of 5-substituted 2-amino-1,3,4-oxadiazoles

A rapid, improved, and environmentally benign synthesis of 5-substituted 2-amino-1,3,4-oxadiazoles by one-pot electrocyclization of acylthiosemicarbazones is reported. Controlled potential electrolysis was performed at room temperature in acetonitrile as