(4-Bromo-2,6-difluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with bromine and fluorine atoms. This compound typically exhibits a white to off-white crystalline solid form. Its molecular structure includes a boron atom bonded to a hydroxyl group and an aromatic ring, which contributes to its reactivity, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The presence of bromine and fluorine substituents can influence its electronic properties and solubility, making it useful in various synthetic applications, including medicinal chemistry and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug delivery systems. The compound's 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.

(4-Bromo-2,6-difluorophenyl)boronic acid

352535-81-0: 4-Bromo-2,6-difluorophenylboronicacid, boronic acid, B-(4-bromo-2,6-difluorophenyl)-, 4-Bromo-2 6-Difluorophenylboronic Acid, 4-Bromo-2,6-difluorophenylboronic acid

4-Bromo-2,6-difluorophenylboronic acid

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CAS 352535-81-0: (4-Bromo-2,6-difluorophenyl)boronic acid

4-Bromo-2,6-difluorophenylboronic acid

Ref: 10-F225456

(4-bromo-2,6-difluorophenyl)boronic Acid

Ref: 3D-FB105782

4-BROMO-2 6-DIFLUOROPHENYLBORONIC ACID

Ref: IN-DA00C0C7

4-Bromo-2,6-difluorobenzeneboronic acid

Ref: 54-PC7580