(2,3-Difluoro-4-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The molecule features two fluorine atoms at the 2 and 3 positions and a methyl group at the 4 position of the phenyl ring, which influences its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. This compound is typically a white to off-white solid and is soluble in polar organic solvents. Its unique substitution pattern can impart specific electronic and steric properties, which may enhance its utility in medicinal chemistry and materials science. Additionally, the presence of fluorine atoms can increase lipophilicity and alter biological activity, making it a subject of interest in drug development and chemical research. Safety data should be consulted for handling and storage, as with all chemical substances.

(2,3-difluoro-4-methylphenyl)boronic acid

508235-16-3: (2,3-Difluoro-4-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The molecule features two fluorine atoms at the 2 and 3 positions and a methyl group at the 4 position of the phenyl ring, which influences its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. This compound is typically a white to off-white solid and is soluble in polar organic solvents. Its unique substitution pattern can impart specific electronic and steric properties, which may enhance its utility in medicinal chemistry and materials science. Additionally, the presence of fluorine atoms can increase lipophilicity and alter biological activity, making it a subject of interest in drug development and chemical research. Safety data should be consulted for handling and storage, as with all chemical substances.

2,3-Difluoro-4-methylphenylboronicacid

<p>2,3-Difluoro-4-methylphenylboronic acid</p>

CAS 508235-16-3

(2,3-difluoro-4-methylphenyl)boronic acid

2,3-Difluoro-4-methylphenylboronicacid

Ref: IN-DA006VPU

2,3-Difluoro-4-methylphenylboronic acid

Ref: 54-PC412133

(2,3-Difluoro-4-methylphenyl)boronic acid

Ref: 10-F209585