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Structure of 4434-13-3
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5-Methylpyridine-2-carboxylic acid features a pyridine core with strategically positioned methyl and carboxylic acid groups, enabling integration into bioactive scaffolds. The electron-deficient heterocycle pairs with the polar carboxylate for enhanced solubility and metal coordination. This robust, bench-stable derivative supports modular synthesis in medicinal chemistry and materials science applications.
5-Methylpyridine-2-carboxylic acid serves as a versatile building block in medicinal chemistry and catalysis, offering a well-defined pyridine scaffold with orthogonal functional handles. The carboxylic acid group enables direct amidation, esterification, or coupling reactions, while the methyl substituent provides a site for selective oxidation or further functionalization. Its stability under standard reaction conditions and compatibility with diverse synthetic transformations make it a practical choice for constructing heterocyclic frameworks and API intermediates.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P280-P501
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Lot numbers can be found on the outside label of a product: