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Structure of 40673-25-4
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4-Chloro-2-hydroxypyridine features a hydroxyl group flanked by a chlorine substituent on a pyridine core, enabling direct participation in cross-coupling and nucleophilic substitution reactions. The ortho-chloro arrangement enhances reactivity toward palladium-catalyzed transformations, while the phenolic OH offers a handle for derivatization. This scaffold delivers high functional group compatibility and stability under standard conditions.
4-Chloro-2-hydroxypyridine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C2 position via nucleophilic substitution or transition-metal-catalyzed coupling. Its hydroxyl group provides a handle for derivatization while maintaining compatibility with common protecting group strategies. Bench-stable and readily purified by recrystallization, it functions effectively in the synthesis of pyridine-based scaffolds relevant to pharmaceutical development.
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Lot numbers can be found on the outside label of a product: