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Structure of 176672-49-4
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4-(tert-Butoxy)phenylboronic acid features a boronic acid handle appended to a para-substituted phenyl ring, where the tert-butoxy group enhances solubility and stability. This bench-stable derivative enables efficient Suzuki-Miyaura cross-coupling reactions under standard conditions, offering reliable access to functionalized biaryls in synthetic and medicinal chemistry workflows.
4-(tert-Butoxy)phenylboronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. Its tert-butoxy group enhances solubility and stability while enabling selective deprotection under mild acidic conditions. The boronic acid functionality facilitates efficient coupling with aryl halides and triflates, making it ideal for constructing biaryl scaffolds in pharmaceutical and materials synthesis.
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Lot numbers can be found on the outside label of a product: