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Structure of 29241-65-4
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5-Bromo-2-chloro-3-pyridinecarboxylic acid features a pyridine ring bearing bromo and chloro substituents at the 5- and 2-positions, respectively, with a carboxylic acid group at the 3-position. This electron-deficient heterocycle serves as a key scaffold for medicinal chemistry applications, offering enhanced metabolic stability and tailored reactivity in cross-coupling transformations.
5-Bromo-2-chloro-3-pyridinecarboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of pyridine-based scaffolds in medicinal chemistry. Its orthogonal halogenation pattern facilitates selective cross-coupling reactions, while the carboxylic acid group supports direct derivatization or activation for amide and ester formation. The compound exhibits excellent bench stability and is compatible with standard purification methods, making it well-suited for iterative synthetic campaigns requiring functional group tolerance and predictable reactivity.
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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: