(2,4-Dibromo-6-fluorophenyl)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 two bromine atoms and one fluorine atom. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. The presence of bromine and fluorine substituents can influence its reactivity and stability, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. The compound's unique electronic properties, stemming from the halogen substitutions, may also affect its biological activity and potential applications in medicinal chemistry. Overall, (2,4-dibromo-6-fluorophenyl)boronic acid is a versatile compound with significant utility in organic synthesis and materials science.

(2,4-dibromo-6-fluorophenyl)boronic acid

870778-96-4: (2,4-Dibromo-6-fluorophenyl)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 two bromine atoms and one fluorine atom. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. The presence of bromine and fluorine substituents can influence its reactivity and stability, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. The compound's unique electronic properties, stemming from the halogen substitutions, may also affect its biological activity and potential applications in medicinal chemistry. Overall, (2,4-dibromo-6-fluorophenyl)boronic acid is a versatile compound with significant utility in organic synthesis and materials science.

CAS 870778-96-4

(2,4-dibromo-6-fluorophenyl)boronic acid

2,4-Dibromo-6-fluorophenylboronic acid

Ref: IN-DA003FPN

2,4-Dibromo-6-fluorophenylboronic acid

Ref: 54-PC412100

(2,4-Dibromo-6-fluorophenyl)boronic acid

Ref: 10-F338097