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Structure of 1784089-67-3
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This imidazopyridine carboxylic acid features a brominated heterocyclic core that enables direct functionalization in cross-coupling reactions. The electron-deficient pyridine ring and pendant carboxylic acid group facilitate integration into bioactive scaffolds, while the bench-stable structure supports reliable handling under standard conditions.
2-Bromoimidazo[1,2-a]pyridine-7-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient construction of imidazo[1,2-a]pyridine scaffolds through palladium-catalyzed cross-coupling reactions. The carboxylic acid group facilitates derivatization via amide bond formation, while the bromine atom provides a reliable handle for further functionalization. Its bench-stable solid form and compatibility with standard synthetic protocols make it well-suited for modular synthesis of 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: