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Structure of 666747-04-2
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3-Bromo-4-(hydroxymethyl)phenol features a phenolic hydroxyl group paired with a reactive bromide and a primary alcohol, enabling sequential functionalization in synthetic sequences. This trifunctional scaffold integrates readily into complex architectures via nucleophilic substitution or coupling reactions under mild conditions. The molecule exhibits favorable solubility in common organic solvents and maintains stability during standard bench handling.
3-Bromo-4-(hydroxymethyl)phenol serves as a versatile building block for medicinal chemistry and materials synthesis, enabling efficient functionalization via Suzuki-Miyaura and Stille couplings. The bromo group facilitates palladium-catalyzed cross-coupling, while the hydroxymethyl and phenolic hydroxyl groups offer orthogonal reactivity for derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses of bioactive heterocycles and polymer precursors.
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Lot numbers can be found on the outside label of a product: