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8-methyl-3-phenyl[1,2,4]triazolo[4,3-a]pyridine is a complex organic compound with the molecular formula C13H10N4. It features a triazolo[4,3-a]pyridine core, which is a fused ring system consisting of a triazole and a pyridine. The compound has a methyl group at the 8th position and a phenyl group at the 3rd position, which are both substituents that can significantly influence its chemical properties and potential applications. This specific arrangement of atoms and functional groups may endow the molecule with unique reactivity or biological activity, making it a subject of interest in fields such as medicinal chemistry and materials science.

4926-17-4

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4926-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4926-17-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4926-17:
(6*4)+(5*9)+(4*2)+(3*6)+(2*1)+(1*7)=104
104 % 10 = 4
So 4926-17-4 is a valid CAS Registry Number.

4926-17-4SDS

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 8-methyl-3-phenyl-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names 8-Methyl-3-phenyl-s-triazolo<4,3-a>pyridin

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:4926-17-4 SDS

4926-17-4Upstream product

4926-17-4Downstream Products

4926-17-4Relevant academic research and scientific papers

An improved synthesis of 3-substituted 1,2,4-triazolo[4,3-a]pyridines and 1,2,4-triazolo[4,3-b]pyridazines

Bourgeois,Cantegril,Chene,Gelin,Mortier,Moyroud

, p. 3195 - 3199 (1993)

The preliminary results of a simple and versatile one-pot procedure for the preparation of 3-substituted 1,2,4-triazolo[4,3-a]pyridines and 1,24,- triazolo[4,3-b]pyridazines are described. Intramolecular cyclization of nitrile imine ylides are carried out

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