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Structure of 1211516-18-5
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6-Bromo-3-methylpyridine-2-carboxylic acid features a pyridine core functionalized with bromo, methyl, and carboxylic acid groups at strategic positions. This configuration enables direct incorporation into diverse synthetic scaffolds, particularly in medicinal chemistry and agrochemical development. The compound exhibits enhanced reactivity in cross-coupling and derivatization reactions due to the electron-withdrawing carboxylate and halogen moieties.
6-Bromo-3-methylpyridine-2-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling direct functionalization at the pyridine core. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid and methyl functionalities offer orthogonal handles for derivatization. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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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: