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1,2,4-Triazolo[4,3-a]pyridine, 3-(2-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5006-54-2

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5006-54-2 Usage

General Description

1,2,4-Triazolo[4,3-a]pyridine, 3-(2-pyridinyl)- is a chemical compound used in pharmaceutical research and development. It is a heterocyclic compound containing a triazolopyridine ring system. 1,2,4-Triazolo[4,3-a]pyridine, 3-(2-pyridinyl)- has shown potential in the treatment of various diseases and conditions due to its ability to interact with and modulate specific biological targets. It is also used as a building block for the synthesis of other organic compounds, making it an important molecule in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 5006-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5006-54:
(6*5)+(5*0)+(4*0)+(3*6)+(2*5)+(1*4)=62
62 % 10 = 2
So 5006-54-2 is a valid CAS Registry Number.

5006-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-pyridin-2-yl-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names triazolopyridine

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:5006-54-2 SDS

5006-54-2Downstream Products

5006-54-2Relevant academic research and scientific papers

Stereoisomerization in Heterocyclic Hydrazones Derived from 2-Acylpyridines and their Oxidative Cyclization with Mercury(II) Acetate and Lead Tetra-acetate to Fused 1,2,4-Triazoles and 1,2,3-Triazolium Systems

Butler, Richard N.,Johnston, Sean M.

, p. 2109 - 2116 (2007/10/02)

Hydrazones prepared by coupling 2-acylpyridines with arylhydrazines were isolated predominantly as E-isomers when the acyl substituent R was small (H or Me).When R was a phenyl group significant yields of Z-isomers, containing an intramolecular hydrogen b

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