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Structure of 25462-98-0
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2-Chloro-6-methylpyridine-4-carbonitrile features a pyridine core functionalized with chlorine, methyl, and nitrile groups at strategic positions, enabling selective coupling in heterocyclic synthesis. The electron-deficient ring facilitates nucleophilic substitution, while the nitrile group serves as a handle for downstream transformations. This compound demonstrates stability under standard bench conditions and compatibility with diverse reaction media.
2-Chloro-6-methylpyridine-4-carbonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of nitrogen-containing heterocycles and functionalized pharmaceutical scaffolds. Its orthogonal reactivity—combining a chloropyridine electrophile with a nitrile group—facilitates palladium-catalyzed couplings and regioselective transformations under mild conditions. The compound exhibits excellent bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for scalable synthesis and medicinal chemistry applications.
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Lot numbers can be found on the outside label of a product: