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Structure of 1159811-32-1
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Methyl 6-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate is a bench-stable heterocyclic ester featuring a brominated triazolopyridine core. This scaffold integrates a reactive halogen site with a polar ester group, enabling direct coupling in cross-coupling reactions and facilitating downstream derivatization in medicinal chemistry and materials synthesis.
Methyl 6-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate serves as a versatile building block for the synthesis of triazolopyridine-based scaffolds. The bromine at the C6 position enables palladium-catalyzed cross-coupling reactions, while the ester group supports further functionalization via hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry campaigns targeting kinase inhibitors and other bioactive heterocycles.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: