6-Bromo-2,3-difluorophenylboronic 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. The molecular structure features a phenyl ring with a bromine atom at the 6-position and two fluorine atoms at the 2 and 3 positions, which contribute to its unique reactivity and properties. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a boron source for the formation of carbon-carbon bonds. The presence of the electron-withdrawing fluorine atoms enhances its reactivity, while the bromine atom can facilitate further functionalization. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. Overall, 6-bromo-2,3-difluorophenylboronic acid is a valuable intermediate in synthetic chemistry due to its versatile reactivity and functional group compatibility.

6-bromo-2,3-difluorophenylboronic acid

870718-10-8: 2-Bromo-5,6-difluorophenylboronic acid

2-BROMO-5,6-DIFLUOROPHENYLBORONIC ACID

6-Bromo-2,3-difluorophenylboronic acid

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CAS 870718-10-8: 6-bromo-2,3-difluorophenylboronic acid

2-BROMO-5,6-DIFLUOROPHENYLBORONIC ACID

Ref: IN-DA003BYM

6-Bromo-2,3-difluorophenylboronic acid

Ref: 54-PC412093

(6-Bromo-2,3-Difluorophenyl)-Boronic Acid

Ref: 3D-FB86660

(6-Bromo-2,3-difluorophenyl)boronic acid

Ref: 10-F225761