Boronic acid, specifically B-(5-amino-2-fluorophenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with an amino group and a fluorine atom. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The amino group contributes to its basicity and potential reactivity in various chemical reactions, including Suzuki coupling, which is a common method for forming carbon-carbon bonds. The fluorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity or altering its interaction with biological targets. Boronic acids are often utilized in medicinal chemistry and materials science due to their ability to form reversible covalent bonds with diols, making them valuable in drug design and sensor applications. Overall, B-(5-amino-2-fluorophenyl)boronic acid is a versatile compound with significant implications in synthetic chemistry and pharmaceutical development.

Boronic acid,B-(5-amino-2-fluorophenyl)-

873566-74-6: Boronic acid, specifically B-(5-amino-2-fluorophenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with an amino group and a fluorine atom. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The amino group contributes to its basicity and potential reactivity in various chemical reactions, including Suzuki coupling, which is a common method for forming carbon-carbon bonds. The fluorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity or altering its interaction with biological targets. Boronic acids are often utilized in medicinal chemistry and materials science due to their ability to form reversible covalent bonds with diols, making them valuable in drug design and sensor applications. Overall, B-(5-amino-2-fluorophenyl)boronic acid is a versatile compound with significant implications in synthetic chemistry and pharmaceutical development.

CAS 873566-74-6

Boronic acid,B-(5-amino-2-fluorophenyl)-

5-Amino-2-fluorophenylboronic acid

Ref: IN-DA003BXM