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Structure of 184416-84-0
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2,3-Dichloro-4-pyridinecarboxylic acid features a pyridine core substituted with two chlorine atoms at the 2 and 3 positions and a carboxylic acid group at the 4 position. This electron-deficient heterocycle serves as a key scaffold for medicinal chemistry, integrating readily into bioactive molecules via amidation or esterification. The dichloro substitution enhances metabolic stability and modulates electronic properties, facilitating targeted interactions in kinase inhibition and receptor binding studies.
2,3-Dichloro-4-pyridinecarboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via coupling and cyclization reactions. Its dichloro substitution pattern enhances electrophilic reactivity at C2 and C3, facilitating nucleophilic aromatic substitution under mild conditions. The carboxylic acid group supports direct derivatization or metal-catalyzed cross-coupling, offering robust functional group tolerance and ease of purification—ideal 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: