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CAS 1268242-41-6

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4-sec-Butylphenylboronic acid pinacol ester

Description:
4-sec-Butylphenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group esterified with pinacol. This compound typically features a phenyl ring substituted with a sec-butyl group, which contributes to its hydrophobic properties and influences its solubility in organic solvents. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The pinacol ester formation enhances the stability of the boronic acid, allowing for easier handling and storage. This compound may exhibit moderate to high reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, its structural characteristics may influence its biological activity, making it a candidate for further research in drug development. Overall, 4-sec-butylphenylboronic acid pinacol ester is a versatile compound with significant implications in synthetic organic chemistry and materials science.
Formula:C16H25BO2
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(1-methylpropyl)phenyl]-
  • 4,4,5,5-tetramethyl-2-(4-sec-butylphenyl)-1,3,2-dioxaborolane
  • 2-(4-(sec-Butyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4-sec-Butylphenylboronic acid pinacol ester
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