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Structure of 1214344-24-7
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2-Chloro-3-methoxypyridine-4-carboxylic acid features a pyridine core functionalized with chlorine, methoxy, and carboxylic acid groups at positions 2, 3, and 4, respectively. This arrangement enables direct incorporation into pharmaceutical intermediates and bioactive molecule scaffolds, where the electron-withdrawing chloride and polar methoxy substituents facilitate regioselective transformations under standard conditions.
2-Chloro-3-methoxypyridine-4-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient coupling reactions via its carboxylic acid and halogen functionalities. The methoxy group provides orthogonality in protecting group strategies, while the chloropyridine moiety facilitates palladium-catalyzed cross-couplings. Bench-stable and readily purified by recrystallization, it supports scalable access to functionalized pyridine scaffolds relevant in medicinal chemistry and agrochemical development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: