Boronic acid, B-(2-cyano-4-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 further substituted with a cyano group (-CN) and a fluorine atom (-F). 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 cyano group contributes to its electron-withdrawing characteristics, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling and other cross-coupling reactions. The fluorine atom can influence the compound's electronic properties and stability. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in organic synthesis and materials science. Overall, this compound's unique functional groups make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.

Boronic acid, B-(2-cyano-4-fluorophenyl)-

876601-43-3: Boronic acid, (2-cyano-4-fluorophenyl)- (9CI), 2-Cyano-4-fluorophenylboronic acid

2-Cyano-4-fluorophenylboronic acid

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CAS 876601-43-3: Boronic acid, B-(2-cyano-4-fluorophenyl)-

2-Cyano-4-fluorophenylboronic acid

Ref: 54-PC412334

(2-cyano-4-fluorophenyl)boronic Acid

Ref: 3D-FC104754

(2-Cyano-4-fluorophenyl)boronic acid

Ref: 10-F234077

2-Cyano-4-fluorobenzeneboronic acid pinacol ester

Ref: IN-DA008E42