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Structure of 7477-10-3
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6-Chloro-5-nitro-3-pyridinecarboxylic acid features a pyridine core functionalized with electron-withdrawing chlorine and nitro groups, enhancing its reactivity in cross-coupling and cyclization processes. This bench-stable derivative delivers high regioselectivity in synthetic routes to bioactive heterocycles.
6-Chloro-5-nitro-3-pyridinecarboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its orthogonal functional groups—chloro, nitro, and carboxylic acid—facilitate sequential transformations under mild conditions, supporting modular diversification in medicinal chemistry campaigns. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for scalable 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: