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Structure of 950846-26-1
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B-(4-Bromo-2,5-dimethoxyphenyl)boronic acid features a boronate moiety attached to a brominated, dimethoxy-substituted phenyl ring, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The electron-rich aromatic system enhances reactivity, while the bench-stable boronic acid functionality simplifies handling and integration into complex molecule synthesis under standard conditions.
B-(4-Bromo-2,5-dimethoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The bromo and dimethoxy substituents provide orthogonal reactivity and enhanced solubility, facilitating downstream functionalization in heterocyclic and pharmaceutical synthesis. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step sequences requiring robust boronic acid handles.
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Lot numbers can be found on the outside label of a product: