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89167-24-8

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89167-24-8 Usage

General Description

6-Bromo[1,2,4]triazolo[1,5-a]pyrimidine is a chemical compound with a fused heterocyclic ring structure. It is a pyrimidine derivative containing a bromine atom and a triazolo ring system. 6-BROMO[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE has potential applications in pharmaceutical chemistry, particularly in the development of new drugs and bioactive molecules due to its unique structure and reactivity. Additionally, it may exhibit biological activity and could be used as a building block in the synthesis of other organic compounds. Further research and investigation into the properties and potential uses of 6-Bromo[1,2,4]triazolo[1,5-a]pyrimidine are necessary to fully understand its capabilities and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89167-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89167-24:
(7*8)+(6*9)+(5*1)+(4*6)+(3*7)+(2*2)+(1*4)=168
168 % 10 = 8
So 89167-24-8 is a valid CAS Registry Number.

89167-24-8SDS

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 6-bromo-[1,2,4]triazolo[1,5-a]pyrimidine

1.2 Other means of identification

Product number -
Other names 6-Brom-s-triazolo<2,3-a>pyrimidin

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:89167-24-8 SDS

89167-24-8Relevant articles and documents

ErbB RECEPTOR INHIBITORS AS ANTI-TUMOR AGENTS

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Page/Page column 183; 184, (2021/09/17)

Provided herein are novel compounds as inhibitors of type I receptor tyrosine kinases, the pharmaceutical compositions comprising one or more of the compounds and salts thereof as an active ingredient, and the use of the compounds and salts thereof in the treatment of hyperproliferative diseases, such as cancer and inflammation, in mammals and especially in humans.

A new route for the synthesis of 6-substituted [1,2,4]triazolo[4,3-a] pyrimidines

Krishnaraj, Thulasiraman,Muthusubramanian, Shanmugam

, p. E68-E70 (2014/11/07)

A new method of generating the fused heterocyclic system with bridgehead nitrogen, triazolo[4,3-a]pyrimidine, from 3-amino-1,2,4-triazole and unsaturated halo acids has been described.

METABOTROPIC GLUTAMATE RECEPTOR MODULATORS

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Page/Page column 39-40, (2011/02/24)

The invention relates to heterocyclic derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are mGluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorders

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