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Structure of 1196157-51-3
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2-Amino-6-bromo-3-pyridinecarboxylic acid features a pyridine core functionalized with amino, bromo, and carboxylic acid groups at strategic positions. This combination enables direct incorporation into heterocyclic scaffolds, serving as a key intermediate in the synthesis of bioactive molecules. The molecule exhibits enhanced solubility and stability under standard reaction conditions.
2-Amino-6-bromo-3-pyridinecarboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling direct functionalization at the 2-amino and 6-bromo positions. Its ortho-directing amino group facilitates regioselective substitutions, while the bromide supports palladium-catalyzed cross-coupling reactions. The carboxylic acid moiety allows for amide formation, esterification, or metal salt preparation, enhancing its utility in medicinal chemistry and API development. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic 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: