Boronic acid, specifically 3-(4-fluorophenoxy)phenyl-boronic acid, is an organic 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 4-fluorophenoxy group. This compound typically exhibits properties associated with 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 presence of the fluorine atom in the para position of the phenoxy group can influence the compound's electronic properties, potentially enhancing its reactivity or selectivity in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. The compound's solubility and stability can vary depending on the solvent and conditions, and it may exhibit moderate to high polarity due to the hydroxyl and ether functionalities. Overall, this compound is of interest in the development of pharmaceuticals and advanced materials.

Boronic acid, [3-(4-fluorophenoxy)phenyl]-

283173-82-0: 3-(4-Fluorophenoxy)phenylboronic acid, Boronic acid, [3-(4-fluorophenoxy)phenyl]-

3-(4-Fluorophenoxy)phenylboronic acid

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CAS 283173-82-0: Boronic acid, [3-(4-fluorophenoxy)phenyl]-

3-(4-Fluorophenoxy)phenylboronic acid

Ref: 10-F623619

3-(4-Fluorophenoxy)phenylboronic acid

Ref: 54-PC412468

3-(4-Fluorophenoxy)phenylboronic acid

Ref: 3D-ILA17382

3-(4-Fluorophenoxy)phenylboronic acid

Ref: IN-DA00BIFC