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Structure of 944896-42-8
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6-Bromoimidazo[1,2-a]pyridine-3-carboxylic acid features a fused heterocyclic core with a bromine substituent at the 6-position and a carboxylic acid group at the 3-position. This combination enables direct coupling in cross-coupling reactions and facilitates conjugation to biomolecules or polymers. The molecule exhibits stability under standard bench conditions and compatibility with diverse reaction media.
6-Bromoimidazo[1,2-a]pyridine-3-carboxylic acid serves as a versatile building block for constructing bioactive heterocyclic scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates derivatization via amide formation or esterification. Its stability under standard synthetic conditions and compatibility with diverse functional groups make it well-suited for medicinal chemistry campaigns targeting kinase inhibitors and CNS modulators.
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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: