B-(3-Ethyl-4-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethyl group and a fluorine atom. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the ethyl and fluorine substituents can influence its reactivity, solubility, and biological activity, potentially enhancing its utility in drug development. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and materials science. Overall, B-(3-Ethyl-4-fluorophenyl)boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.

B-(3-Ethyl-4-fluorophenyl)boronic acid

960235-01-2: Boronic acid, B-(3-ethyl-4-fluorophenyl)-, B-(3-Ethyl-4-fluorophenyl)boronic acid

CAS 960235-01-2: B-(3-Ethyl-4-fluorophenyl)boronic acid

3-Ethyl-4-fluorophenylboronic acid

Ref: 54-PC99033

(3-Ethyl-4-fluorophenyl)boronic acid

Ref: 3D-KNB23501

(3-Ethyl-4-fluorophenyl)boronicacid

Ref: IN-DA01M4VW