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Structure of 886362-00-1
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3-Bromoimidazo[1,2-a]pyridine-6-carboxylic acid features a fused heterocyclic core with a bromine atom at the 3-position and a carboxylic acid group at the 6-position. This combination enables direct functionalization in cross-coupling reactions and facilitates conjugation to biomolecules or polymers. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions, making it suitable for use in medicinal chemistry and materials synthesis workflows.
3-Bromoimidazo[1,2-a]pyridine-6-carboxylic acid serves as a versatile building block for constructing biologically active heterocyclic scaffolds. The carboxylic acid functionality enables direct amidation or esterification, while the bromo group facilitates palladium-catalyzed cross-coupling reactions. Its stability under standard bench conditions and compatibility with diverse functional groups make it suitable for iterative synthesis in medicinal chemistry and process development 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: