CAS 216393-64-5: 4-Bromo-2-fluorobenzeneboronic acid

Description: 4-Bromo-2-fluorobenzeneboronic acid is an organoboron compound characterized by the presence of both bromine and fluorine substituents on a benzene ring, along with a boronic acid functional group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group, which can form hydrogen bonds. The presence of the bromine and fluorine atoms introduces unique electronic properties, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. The boronic acid functionality allows for the formation of stable complexes with diols, which is advantageous in applications such as drug development and materials science. Additionally, 4-Bromo-2-fluorobenzeneboronic acid may exhibit interesting reactivity patterns due to the electron-withdrawing effects of the halogen substituents, influencing its behavior in organic synthesis and catalysis. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.

Formula: C₆H₅BBrFO₂

InChI: InChI=1/C6H5BBrFO2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,10-11H

Synonyms:

• 4-Bromo-2-fluorophenylboronic acid

4-Bromo-2-fluorobenzeneboronic acid

CAS: 216393-64-5

• Formula: C₆H₅BBrFO₂
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 218.8161

4-Bromo-2-fluorobenzeneboronic acid

CAS: 216393-64-5

• Purity: 95.0%
• Color and Shape: Solid
• Molecular weight: 218.82000732421875

4-Bromo-2-fluorobenzeneboronic acid

CAS: 216393-64-5

• Purity: 98%
• Color and Shape: White Solid
• Molecular weight: 218.82g/mol

4-Bromo-2-Fluorobenzeneboronic Acid

CAS: 216393-64-5

4-Bromo-2-fluorobenzeneboronic acid is a boronic acid that can be used in the chemical modification of …

• Formula: C₆H₅BBrFO₂
• Purity: Min. 95%
• Molecular weight: 218.82 g/mol