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5-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRIDINE is an organic heterocyclic compound characterized by a molecular formula of C6H4ClN5. It features a triazole ring fused to a pyridine ring, with a chlorine atom attached at the 5 position of the triazole ring. 5-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRIDINE is recognized for its potential in the pharmaceutical industry as a building block for synthesizing biologically active compounds.

27187-13-9

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27187-13-9 Usage

Uses

Used in Pharmaceutical Industry:
5-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRIDINE is used as a building block for the synthesis of various biologically active compounds, including fungicides, herbicides, and insecticides. Its unique structure contributes to the development of new pharmaceuticals with potential applications in treating a range of diseases.
Used in Research and Development:
5-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRIDINE serves as a research reagent, facilitating the exploration of new chemical entities and their potential therapeutic effects. It is instrumental in chemical biology research, aiding scientists in understanding the interactions between small molecules and biological targets.
Used in Chemical Biology Research:
5-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRIDINE is utilized as a tool in chemical biology to study the mechanisms of action of drugs and their effects on biological systems. Its structural features make it a valuable probe for investigating molecular recognition and signaling pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 27187-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,8 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27187-13:
(7*2)+(6*7)+(5*1)+(4*8)+(3*7)+(2*1)+(1*3)=119
119 % 10 = 9
So 27187-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClN3/c7-5-2-1-3-6-9-8-4-10(5)6/h1-4H

27187-13-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H63881)  5-Chloro-1,2,4-triazolo[4,3-a]pyridine, 97%   

  • 27187-13-9

  • 250mg

  • 460.0CNY

  • Detail
  • Alfa Aesar

  • (H63881)  5-Chloro-1,2,4-triazolo[4,3-a]pyridine, 97%   

  • 27187-13-9

  • 1g

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H63881)  5-Chloro-1,2,4-triazolo[4,3-a]pyridine, 97%   

  • 27187-13-9

  • 5g

  • 6125.0CNY

  • Detail

27187-13-9SDS

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 5-chloro-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names 5-Chlor-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:27187-13-9 SDS

27187-13-9Relevant academic research and scientific papers

Synthesis and studies on the anticonvulsant activity of 5-alkoxy-[1,2,4]triazolo[4,3-a]pyridine derivatives

Guan,Zhang,Sun,Chang,Sui

, p. 372 - 377 (2012/10/29)

In this study, a series of new 5-alkoxy-[1,2,4]triazolo[4,3-a]pyridine derivatives was synthesized and their anticonvulsant activity and neurotoxicity was evaluated with the maximal electroshock and rotarod tests, respectively. The most promising compounds, 3p (5-(4-chlorophenoxy)-[1,2,4]triazolo[4,3-a] pyridine) and 3r (5-(4-bromophenoxy)-[1,2,4]triazolo[4,3-a]pyridine), showed a median effective dose of 13.2 and 15.8 mg/kg and had a protective index value of 4.8 and 6.9, respectively. For exploring the putative mechanism of action, compounds 3n, 3p and 3r were tested in chemically induced models. Georg Thieme Verlag KG Stuttgart.New York.

2-AMINOPYRIDINE ANALOGS AS GLUCOKINASE ACTIVATORS

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Page/Page column 119, (2008/12/04)

Provided are compounds that are useful in the treatment and/or prevention of diseases mediated by deficient levels of glucokinase activity, such as diabetes mellitus. Also provided are methods of treating or preventing diseases and disorders characterized by underactivity of glucokinase or which can be treated by activating glucokinase.

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