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Structure of 1805479-11-1
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2-Bromo-5-chloro-3-fluorophenol features a trifluorinated aromatic core with strategically positioned halogens enabling precise functionalization in pharmaceutical intermediates. This electron-deficient phenol integrates readily into coupling reactions, offering enhanced reactivity under standard conditions. The ortho-bromo and meta-chloro substituents provide complementary handles for diversification, while the phenolic OH group supports direct derivatization.
2-Bromo-5-chloro-3-fluorophenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling regioselective functionalization via palladium-catalyzed cross-coupling reactions. Its ortho-halogenated framework provides enhanced reactivity for Suzuki, Stille, and Negishi couplings, while the phenolic hydroxyl group offers a handle for derivatization. Bench-stable and readily purified by recrystallization, it functions as a key intermediate in the construction of complex heterocyclic scaffolds and bioactive molecules.
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Lot numbers can be found on the outside label of a product: