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CAS 156635-88-0

:

4-Benzyloxy-3,5-difluorophenylboronic acid

Description:
4-Benzyloxy-3,5-difluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with two fluorine atoms at the 3 and 5 positions, enhancing its electronic properties and potentially influencing its reactivity. The benzyloxy group at the para position provides steric hindrance and can affect the solubility and stability of the compound. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of fluorine atoms can impart unique characteristics such as increased lipophilicity and altered biological activity. Overall, 4-Benzyloxy-3,5-difluorophenylboronic acid is a versatile compound with significant implications in synthetic organic chemistry and pharmaceutical development.
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