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Structure of 929000-66-8
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3-Bromo-6-chloropyridine-2-carboxylic acid features a pyridine core functionalized with bromo, chloro, and carboxylic acid groups at strategic positions, enabling direct incorporation into cross-coupling and bioconjugation workflows. The electron-deficient ring enhances reactivity in palladium-catalyzed transformations, while the carboxylic acid facilitates derivatization or salt formation for improved solubility and handling.
3-Bromo-6-chloropyridine-2-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen functionality. The carboxylic acid group facilitates direct derivatization or activation for amide bond formation, while the bromo and chloro substituents provide complementary reactivity for sequential functionalization. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for 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: