Boronic acid, specifically 3,4-bis(2-methylbutoxy)phenyl-, 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 two 2-methylbutoxy groups. This structure imparts unique properties, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The boronic acid moiety allows for reversible covalent bonding with diols, which is significant in the development of sensors and drug delivery systems. The presence of the bulky 2-methylbutoxy groups enhances the solubility of the compound in organic solvents and may influence its reactivity and stability. Additionally, boronic acids are known for their role in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their potential in pharmaceutical applications.

Boronic acid, [3,4-bis(2-methylbutoxy)phenyl]-

340148-67-6: 3,4-Bis(2-methylbutoxy)benzeneboronic acid, Boronic acid, [3,4-bis(2-methylbutoxy)phenyl]-, [3,4-Bis(2-methylbutoxy)phenyl]boronic acid, boronic acid, B-[3,4-bis(2-methylbutoxy)phenyl]-, 3,4-Bis(2-methylbutyloxy)benzeneboronic acid

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CAS 340148-67-6: Boronic acid, [3,4-bis(2-methylbutoxy)phenyl]-

3,4-Bis(2-methylbutyloxy)benzeneboronicacid

Ref: 3D-FB150735

3,4-Bis(2-methylbutyloxy)benzeneboronic acid

Ref: IN-DA00CNB3