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7-Bromo[1,2,4]triazolo[4,3-a]pyridine is a heterocyclic chemical compound characterized by a molecular formula of C5H3BrN4. It features a triazolopyridine ring system with a bromine substituent at the 7-position, which endows it with unique structural and biological properties. 7-Bromo[1,2,4]triazolo[4,3-a]pyridine holds promise in the realm of medicinal chemistry and drug discovery due to its distinctive attributes.

832735-60-1

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832735-60-1 Usage

Uses

Used in Medicinal Chemistry:
7-Bromo[1,2,4]triazolo[4,3-a]pyridine is utilized as a key intermediate in the synthesis of novel pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Drug Discovery:
7-Bromo[1,2,4]triazolo[4,3-a]pyridine serves as a valuable building block in organic synthesis, contributing to the creation of innovative molecules with potential medicinal properties. Its presence in synthesized compounds may enhance their efficacy and selectivity in targeting specific biological pathways.
Used in Scientific Research:
7-Bromo[1,2,4]triazolo[4,3-a]pyridine's potential biological activities make it an intriguing subject for further research and development across various scientific disciplines. Its exploration may lead to the discovery of new mechanisms of action and applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 832735-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,7,3 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 832735-60:
(8*8)+(7*3)+(6*2)+(5*7)+(4*3)+(3*5)+(2*6)+(1*0)=171
171 % 10 = 1
So 832735-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrN3/c7-5-1-2-10-4-8-9-6(10)3-5/h1-4H

832735-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Bromo-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names 7-bromo-[1,2,4]triazolo[4,3-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:832735-60-1 SDS

832735-60-1Relevant academic research and scientific papers

HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS AND COMBINATIONS THEREOF

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Page/Page column 125, (2015/07/07)

Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds and combinations of such compounds and other therapeutic agents.

HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS

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Page/Page column 110, (2014/01/18)

Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds.

CYCLIC INHIBITORS OF 11 β-HYDROXYSTEROID DEHYDROGENASE 1

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Page/Page column 71, (2010/08/18)

This invention relates to novel compounds of the Formula Formulas (I), (Ia1-20), (Ib1-20), (Ic1-20), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.

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