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Structure of 886365-46-4
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5-Chloro-3-methylpyridine-2-carboxylic acid features a pyridine core functionalized with chlorine, methyl, and carboxylic acid groups at strategic positions. This electron-deficient scaffold enables direct incorporation into bioactive molecules and pharmaceutical intermediates. The carboxylic acid moiety facilitates derivatization under standard coupling conditions. The compound exhibits bench-stable handling and compatibility with diverse synthetic transformations.
5-Chloro-3-methylpyridine-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocycles through established functional group transformations. Its ortho-carboxylic acid and meta-chloro substituents provide orthogonal reactivity for coupling, derivatization, and cyclization processes. Bench-stable and amenable to standard purification methods, it functions reliably in the synthesis of pharmaceutical intermediates and agrochemical scaffolds.
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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: