80980-09-2

Basic information

• Product Name: 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE
• Synonyms: 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE;3-(3-Phenyl-1H-1,2,4-triazol-5-yl)pyridine
• CAS NO: 80980-09-2
• Molecular Formula: C₁₃H₁₀N₄
• Molecular Weight: 222.2453
• Mol File: 80980-09-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 472.7°C at 760 mmHg
• Flash Point: 226.2°C
• Appearance: /
• Density: 1.248g/cm³
• Vapor Pressure: 4.2E-09mmHg at 25°C
• Refractive Index: 1.64
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE(80980-09-2)
• EPA Substance Registry System: 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE(80980-09-2)

Safety Data

• Hazardous Substances Data: 80980-09-2(Hazardous Substances Data)

Usage

General Description

3-(5-Phenyl-4H-1,2,4-triazol-3-yl)pyridine is a chemical compound with the molecular formula C15H11N5. It is a heterocyclic compound containing a pyridine ring and a 1,2,4-triazole ring with a phenyl group attached to the triazole ring. 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE is commonly used in the field of medicinal chemistry as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure and properties make it an important intermediate in the production of diverse organic compounds. Additionally, 3-(5-phenyl-4H-1,2,4-triazol-3-yl)pyridine has potential applications in the development of new drugs and materials due to its pharmacological and chemical properties.

InChI:InChI=1/C13H10N4/c1-2-5-10(6-3-1)12-15-13(17-16-12)11-7-4-8-14-9-11/h1-9H,(H,15,16,17)

Upstream product

• 100-54-9 pyridine-3-carbonitrile 
• 553-53-7 Nicotinic acid hydrazide 
• 100-52-7 benzaldehyde 
• 14157-55-2 N¹-(α-Aminobenzyliden)-3-pyridincarboxamidrazon 

Relevant articles and documents

Synthesis and QSAR studies of some novel disubstituted 1,2,4-triazoles as antimicrobial agents

Disubstituted 1,2,4-triazoles 3a-k, 4a-k, and 6a-k have been synthesized from anthranilic acid and nicotinic acid, respectively, through a multi-step reaction sequence via their hydrazides. Synthesized compounds were evaluated for their in vitro antimicro

Metallhydrazide, XIX. Addition bis(diethylaluminio)substituierter Amidrazone und Carbohydrazide an Nitrile

Amidrazones and carbohydrazides react with two equivalents of triethylaluminium to give bis(diethylaluminio) derivatives 1 and 7, respectively.In contrast to the corresponding mono(diethylaluminio) derivatives or disodium salts, these are capable of addit