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Structure of 1082066-52-1
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This boronic acid features a fluorinated aryl ring paired with a hydroxymethyl handle, enabling efficient coupling in Suzuki-Miyaura reactions. The electron-deficient aromatic system enhances reactivity while maintaining bench-stable handling under standard conditions.
(3-Fluoro-4-(hydroxymethyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-fluoro substituent enhances regioselectivity and metabolic stability, while the boronic acid and hydroxymethyl groups offer orthogonal reactivity for downstream functionalization. Bench-stable and readily purified by recrystallization, it facilitates streamlined synthesis of fluorinated aryl scaffolds relevant to medicinal chemistry and materials science.
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Lot numbers can be found on the outside label of a product: