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Structure of 1190322-26-9
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This pyrrolopyridine carboxylic acid features a brominated heterocycle with a reactive carboxyl group, enabling direct coupling in cross-coupling and amide formation reactions. The electron-deficient aromatic core enhances reactivity in transition-metal catalyzed processes, while the bench-stable structure facilitates handling under standard conditions.
5-Bromo-1H-pyrrolo[2,3-b]pyridine-6-carboxylic acid serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient late-stage functionalization via Pd-catalyzed cross-coupling. The carboxylic acid group facilitates direct derivatization or amide formation, while the bromo substituent provides a reliable handle for further diversification. Bench-stable and compatible with standard purification methods, it functions effectively in medicinal chemistry campaigns targeting kinase inhibitors and other nitrogen-containing scaffolds.
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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: