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Structure of 1234616-71-7
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This pyrrolopyridine carboxylic acid features a brominated heterocyclic core with a pendant carboxylic acid group, enabling direct incorporation into bioactive scaffolds. The electron-deficient ring system facilitates cross-coupling reactions, while the carboxylic acid serves as a handle for derivatization. Bench-stable and moisture-tolerant, it supports efficient synthesis in medicinal chemistry workflows.
4-Bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into heterocyclic scaffolds via cross-coupling and functional group transformations. The carboxylic acid moiety facilitates derivatization through amide formation or esterification, while the bromine substituent supports palladium-catalyzed coupling reactions. Bench-stable and compatible with standard purification methods, it functions effectively in the synthesis of kinase inhibitors and other bioactive molecules.
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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: