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Structure of 461663-79-6
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5-Bromo-1-benzofuran-3-carboxylic acid integrates a bromine substituent at the 5-position of the benzofuran core, delivering enhanced reactivity for cross-coupling transformations. The carboxylic acid group enables direct derivatization or salt formation, while the planar heterocyclic framework ensures compatibility with transition metal catalysis. This scaffold combines synthetic versatility with structural rigidity, supporting applications in medicinal chemistry and materials science.
5-Bromo-1-benzofuran-3-carboxylic acid serves as a versatile building block for the synthesis of functionalized benzofuran scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates derivatization via amide formation or esterification. Its stability under standard bench conditions and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry and materials applications.
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Lot numbers can be found on the outside label of a product: