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1131410-85-9

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1131410-85-9 Usage

General Description

7-Chloro-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine is a chemical compound recognized by its systematic name. The unique aspect of this compound is its structure, which includes a triazolo and pyridin group, both of which are common in pharmaceutical drugs due to their heterocyclic nature. This chemical has yet not as such been investigated thoroughly for any specific pharmacological activity, bioactivity or industrial application. Its properties and implications are largely unexplored, making it a potential subject for future chemical, pharmaceutical or bio-chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 1131410-85-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,1,4,1 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1131410-85:
(9*1)+(8*1)+(7*3)+(6*1)+(5*4)+(4*1)+(3*0)+(2*8)+(1*5)=89
89 % 10 = 9
So 1131410-85-9 is a valid CAS Registry Number.

1131410-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-7-chloro-[1,2,4]triazolo[1,5-a]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:1131410-85-9 SDS

1131410-85-9Relevant articles and documents

TRIAZOLOPYRIDINE COMPOUNDS USEFUL AS PESTICIDES

-

, (2022/01/12)

The present disclosure provides a novel triazolopyridine compound as represented by formula (I) or a salt thereof that controls pests: wherein, R1 and R3 independently represent hydrogen, or the like; R2 represents C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, or the like; R4, R5, R7, and R8 independently represent hydrogen, halogen, or the like; R6 represents C1-C6 haloalkoxy, or the like; and Z represents an oxygen atom, a sulfur atom, SO, or SO2.

NOVEL COMPOUNDS FOR THE TREATMENT OF CANCER

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, (2015/01/09)

The present invention relates to novel compounds showing an inhibitory effect on Mps-1 kinase, to methods of preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds, to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, as well as to intermediate compounds useful in the preparation of said compounds.

DNA gyrase (GyrB)/topoisomerase IV (ParE) inhibitors: Synthesis and antibacterial activity

East, Stephen P.,White, Clara Bantry,Barker, Oliver,Barker, Stephanie,Bennett, James,Brown, David,Boyd, E. Andrew,Brennan, Christopher,Chowdhury, Chandana,Collins, Ian,Convers-Reignier, Emmanuelle,Dymock, Brian W.,Fletcher, Rowena,Haydon, David J.,Gardiner, Mihaly,Hatcher, Stuart,Ingram, Peter,Lancett, Paul,Mortenson, Paul,Papadopoulos, Konstantinos,Smee, Carol,Thomaides-Brears, Helena B.,Tye, Heather,Workman, James,Czaplewski, Lloyd G.

scheme or table, p. 894 - 899 (2009/08/15)

The synthesis and antibacterial activities of three chemotypes of DNA supercoiling inhibitors based on imidazolo[1,2-a]pyridine and [1,2,4]triazolo[1,5-a]pyridine scaffolds that target the ATPase subunits of DNA gyrase and topoisomerase IV (GyrB/ParE) is reported. The most potent scaffold was selected for optimization leading to a series with potent Gram-positive antibacterial activity and a low resistance frequency.

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