(2-Bromo-4,5-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 and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. The presence of the 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 delivery systems. The compound's unique electronic properties, derived from the halogen substituents, may also enhance its utility in medicinal chemistry and materials science. Overall, (2-bromo-4,5-difluorophenyl)boronic acid is a versatile building block in organic synthesis and has potential applications in pharmaceuticals and advanced materials.

(2-bromo-4,5-difluorophenyl)boronic acid

849062-34-6: (2-Bromo-4,5-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 and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. The presence of the 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 delivery systems. The compound's unique electronic properties, derived from the halogen substituents, may also enhance its utility in medicinal chemistry and materials science. Overall, (2-bromo-4,5-difluorophenyl)boronic acid is a versatile building block in organic synthesis and has potential applications in pharmaceuticals and advanced materials.

CAS 849062-34-6

(2-bromo-4,5-difluorophenyl)boronic acid

(2-Bromo-4,5-difluorophenyl)boronic acid

Ref: IN-DA003GNM

2-Bromo-4,5-difluorobenzeneboronic acid

Ref: 54-PC56674

(2-Bromo-4,5-difluorophenyl)boronic acid

Ref: 10-F338287