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Structure of 1159831-86-3
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6-Bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid features a rigid, electron-deficient heterocyclic core that integrates seamlessly into bioactive molecule scaffolds. The carboxylic acid group enables direct coupling reactions, while the bromine substituent offers a strategic handle for palladium-catalyzed cross-couplings. This compound serves as a key building block in medicinal chemistry campaigns targeting kinase inhibitors and other targeted therapeutics.
6-Bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling direct functionalization at the triazolopyridine core. The bromo and carboxylic acid groups offer orthogonal reactivity—facilitating palladium-catalyzed cross-coupling and amide formation—while maintaining bench stability and compatibility with standard purification methods. Its well-defined structure supports efficient incorporation into pharmaceutical scaffolds and advanced intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: