3-(Isobutanoyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with an isobutanoyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and medicinal chemistry. The isobutanoyl group contributes to its hydrophobic characteristics, potentially influencing its solubility and reactivity in different solvents. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. The compound may also exhibit unique reactivity due to the steric and electronic effects imparted by the isobutanoyl substituent. Overall, 3-(Isobutanoyl)phenylboronic acid is a versatile compound with potential applications in drug development and materials science, owing to its functional groups and reactivity profile.

3-(Isobutanoy)phenylboronic acid

2377608-31-4: 3-(Isobutanoyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with an isobutanoyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and medicinal chemistry. The isobutanoyl group contributes to its hydrophobic characteristics, potentially influencing its solubility and reactivity in different solvents. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. The compound may also exhibit unique reactivity due to the steric and electronic effects imparted by the isobutanoyl substituent. Overall, 3-(Isobutanoyl)phenylboronic acid is a versatile compound with potential applications in drug development and materials science, owing to its functional groups and reactivity profile.

CAS 2377608-31-4

3-(Isobutanoy)phenylboronic acid

3-(Isobutanoy)phenylboronic acid

Ref: 54-OR906044