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CAS 957061-15-3

:

6-Bromo-2-fluoro-3-methylphenylboronic acid

Description:
6-Bromo-2-fluoro-3-methylphenylboronic 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, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom at the 6-position, a fluorine atom at the 2-position, and a methyl group at the 3-position, contributing to its unique reactivity and properties. The presence of both halogen substituents (bromine and fluorine) can influence the electronic properties of the molecule, potentially enhancing its reactivity in cross-coupling reactions. Additionally, the boronic acid group allows for participation in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. This compound may also exhibit interesting biological activities, making it a candidate for further research in drug development. Its solubility and stability in various solvents can vary, which is an important consideration for its practical applications.
Formula:C7H7BBrFO2
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