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3-(5-Phenyl-4H-1,2,4-triazol-3-yl)pyridine is a heterocyclic chemical compound with the molecular formula C15H11N5. It features a pyridine ring fused with a 1,2,4-triazole ring, with a phenyl group attached to the triazole moiety. 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE is recognized for its unique structure and properties, making it a significant intermediate in the synthesis of a variety of organic compounds and biologically active molecules, particularly in the field of medicinal chemistry.

80980-09-2

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80980-09-2 Usage

Uses

Used in Medicinal Chemistry:
3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE is used as a building block for the synthesis of pharmaceuticals and biologically active molecules due to its versatile chemical structure and potential to be incorporated into diverse molecular frameworks.
Used in Drug Development:
In the pharmaceutical industry, 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE is utilized as a key intermediate in the development of new drugs, leveraging its pharmacological properties to create novel therapeutic agents with potential applications in treating various diseases and conditions.
Used in Material Science:
Beyond its medicinal applications, 3-(5-PHENYL-4H-1,2,4-TRIAZOL-3-YL)PYRIDINE also holds promise in material science, where its chemical properties may contribute to the creation of new materials with specialized functions, such as in sensors, catalysts, or other advanced technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 80980-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,8 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80980-09:
(7*8)+(6*0)+(5*9)+(4*8)+(3*0)+(2*0)+(1*9)=142
142 % 10 = 2
So 80980-09-2 is a valid CAS Registry Number.
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)

80980-09-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5-phenyl-1H-1,2,4-triazol-3-yl)pyridine

1.2 Other means of identification

Product number -
Other names 3-(5-Phenyl-4H-1,2,4-triazol-3-yl)pyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80980-09-2 SDS

80980-09-2Downstream Products

80980-09-2Relevant academic research and scientific papers

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

Panda, Siva S.,Jain, Subhash C.

, p. 848 - 861 (2014)

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

Synthesis and analgesic activity of new pyridine-based heterocyclic derivatives

Nigade, Ganesh,Chavan, Pradeep,Deodhar, Meenakshi

experimental part, p. 27 - 37 (2012/06/01)

A series of new heterocyclic derivatives having a pyridine nucleus were synthesized. 4-(5-(2-Chlorophenyl)- 4H-1,2,4-triazol-3-yl)pyridine (7c) and 4-(5-(2- Nitrophenyl)-4H-1,2,4-triazol-3-yl)pyridine (7d) presented the best analgesic profie of this series in hot-plate, tail-flick, and formalin-induced licking tests, which was partially prevented by pretreatment with mecamylamine, a nicotinic receptor antagonist. Springer Science+Business Media, LLC 2010.

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

Kauffmann, Thomas,Ban, Laszlo,Kuhlmann, Dieter

, p. 3684 - 3690 (2007/10/02)

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

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