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Structure of 1780644-81-6
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This boronate-functionalized heterocycle integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tert-butyl group enhances solubility and steric protection, while the bromine moiety enables selective cross-coupling. This bench-stable compound delivers efficient access to complex aryl-thiophene architectures in medicinal chemistry and materials synthesis.
3-Bromo-5-(tert-butyl)benzo[b]thiophene serves as a versatile building block for the synthesis of functionalized heterocyclic scaffolds. The bromine substituent enables reliable palladium-catalyzed cross-coupling reactions, while the sterically hindered tert-butyl group enhances bench stability and minimizes unwanted side reactions. This compound functions effectively in standard Suzuki, Stille, and Negishi coupling protocols, facilitating efficient access to complex biaryl and polyheteroaryl architectures relevant to medicinal chemistry and materials science.
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Lot numbers can be found on the outside label of a product: