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Structure of 1216475-30-7
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8-Bromo-[1,2,4]triazolo[4,3-a]pyridine-6-carboxylic acid features a brominated triazolopyridine core paired with a carboxylic acid handle, enabling direct conjugation in medicinal chemistry. The electron-deficient heterocycle facilitates transition metal-catalyzed coupling reactions, while the bench-stable functionality supports modular synthesis of bioactive compounds under standard conditions.
8-Bromo-[1,2,4]triazolo[4,3-a]pyridine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical research. The molecule combines a brominated triazolopyridine core with a carboxylic acid functionality, enabling direct coupling reactions and derivatization via amide formation or esterification. Its bench-stable nature and compatibility with standard cross-coupling protocols facilitate efficient synthesis of complex scaffolds in drug discovery workflows.
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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: