192642-77-6 Usage
General Description
5-Bromo-1,2,3-triazolo[1,5-a]pyridine is a chemical compound with the molecular formula C5H3BrN4. It is a heterocyclic compound that contains a triazole ring fused to a pyridine ring with a bromine atom attached to the triazole ring. 5-BROMO-1,2,3-TRIAZOLO[1,5-A]PYRIDINE is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has been studied for its potential antifungal and antibacterial properties, as well as its use as a precursor in the preparation of various biologically active compounds. Additionally, 5-bromo-1,2,3-triazolo[1,5-a]pyridine has been investigated for its potential applications in materials science and as a tool for chemical biology research.
Check Digit Verification of cas no
The CAS Registry Mumber 192642-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,6,4 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 192642-77:
(8*1)+(7*9)+(6*2)+(5*6)+(4*4)+(3*2)+(2*7)+(1*7)=156
156 % 10 = 6
So 192642-77-6 is a valid CAS Registry Number.
192642-77-6Relevant articles and documents
HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS AND COMBINATIONS THEREOF
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Page/Page column 123, (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.
Triazolopyridines. 18.1 nucleophilic substitution reactions on triazolopyridines; a new route to 2,2'-Bipyridines
Jones, Gurnos,Pitman, Mark A.,Lunt, Edward,Lythgoe, David J.,Abarca, Belen,Ballesteros, Rafael,Elmasnaouy, Mostafa
, p. 8257 - 8268 (2007/10/03)
The synthesis of some 5-, 6-, and 7-halogenotriazolopyridines is described and their reactions with nucleophiles. The formation or 7,7'-bitriazolopyridines provides a new synthesis of 2,2'-bipyridines.