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Structure of 343781-49-7
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2,4-Dichloro-5-iodopyridine is a halogenated pyridine derivative featuring complementary reactive sites for cross-coupling and functionalization. The electron-deficient ring facilitates palladium-catalyzed reactions, while the iodine moiety enables selective C–C bond formation. This compound serves as a key building block in medicinal chemistry and agrochemical synthesis, offering high reactivity under mild conditions.
2,4-Dichloro-5-iodopyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The iodine moiety facilitates efficient Suzuki, Stille, or Negishi couplings, while the dichloro substitution pattern allows for selective functionalization. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing complex pyridine-based scaffolds in API development and materials science applications.
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Lot numbers can be found on the outside label of a product: