[4-(Difluoromethoxy)phenyl]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 a difluoromethoxy group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar organic solvents. The difluoromethoxy group enhances its electronic properties, making it useful in various applications, particularly in medicinal chemistry and materials science. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is significant in the development of sensors and drug delivery systems. Additionally, this compound may participate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of complex organic molecules. Its reactivity and functionalization potential make it a valuable intermediate in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper laboratory practices are followed.

[4-(difluoromethoxy)phenyl]boronic acid

688810-12-0: boronic acid, B-[4-(difluoromethoxy)phenyl]-, 4-Difluoromethoxyphenylboronic acid, 4-Difluoromethoxy-Phenylboronic Acid

(4-(Difluoromethoxy)phenyl)boronic acid

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CAS 688810-12-0: [4-(difluoromethoxy)phenyl]boronic acid

(4-(Difluoromethoxy)phenyl)boronic acid

Ref: IN-DA0033TB

4-(Difluoromethoxy)phenylboronic acid

Ref: 3D-FD84580

4-(Difluoromethoxy)benzeneboronic acid

Ref: 54-PC1431