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Structure of 55304-85-3
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2,6-Dibromo-3-pyridinecarboxylic acid features a pyridine ring bearing bromine substituents at the 2 and 6 positions, which enhance electrophilic reactivity and facilitate downstream coupling reactions. The carboxylic acid group provides a handle for amide formation or metal chelation. This configuration delivers high stability under standard bench conditions and enables precise functionalization in synthetic sequences requiring halogenated heterocyclic scaffolds.
2,6-Dibromo-3-pyridinecarboxylic acid serves as a versatile building block for the synthesis of brominated pyridine scaffolds in medicinal chemistry and materials science. Its dual bromine substituents enable efficient Pd-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates derivatization via amide or ester formation. The compound exhibits good bench stability and is compatible with standard purification techniques, enabling reliable use in multi-step syntheses.
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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: