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Structure of 84703-18-4
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5-Bromo-2-chloro-6-methylnicotinonitrile features a trifunctional pyridine core with complementary reactivity at the bromo, chloro, and nitrile positions. This electron-deficient scaffold enables selective cross-coupling and nucleophilic substitution under mild conditions, offering efficient access to complex heterocyclic architectures in medicinal chemistry and materials synthesis.
5-Bromo-2-chloro-6-methylnicotinonitrile serves as a versatile building block in medicinal chemistry, enabling the construction of substituted pyridine scaffolds via palladium-catalyzed cross-coupling reactions. The molecule’s orthogonal halogenation pattern—bromine at C5 and chlorine at C2—allows for sequential functionalization with high chemoselectivity. The nitrile group provides a handle for downstream transformations, including hydrolysis to carboxylic acids or reduction to aldehydes. Bench-stable and readily purified by column chromatography, it facilitates efficient synthesis of complex heterocyclic intermediates.
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Lot numbers can be found on the outside label of a product: