3,5-Dimethyl-4-chlorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound features a phenyl ring substituted with two methyl groups at the 3 and 5 positions and a chlorine atom at the 4 position, 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 Suzuki coupling reactions for the formation of carbon-carbon bonds. The presence of the chlorine atom can enhance the electrophilicity of the aromatic system, while the methyl groups can provide steric hindrance and influence the compound's overall reactivity. Additionally, 3,5-dimethyl-4-chlorophenylboronic acid may exhibit unique properties in terms of solubility in organic solvents and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its specific characteristics, such as melting point, boiling point, and solubility, would typically be determined through experimental methods.

3,5-DIMETHYL-4-CHLOROPHENYLBORONIC ACID

1056475-86-5: 3,5-Dimethyl-4-chlorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound features a phenyl ring substituted with two methyl groups at the 3 and 5 positions and a chlorine atom at the 4 position, 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 Suzuki coupling reactions for the formation of carbon-carbon bonds. The presence of the chlorine atom can enhance the electrophilicity of the aromatic system, while the methyl groups can provide steric hindrance and influence the compound's overall reactivity. Additionally, 3,5-dimethyl-4-chlorophenylboronic acid may exhibit unique properties in terms of solubility in organic solvents and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its specific characteristics, such as melting point, boiling point, and solubility, would typically be determined through experimental methods.

3,5-Dimethyl-4-chlorophenylboronic acid

<p>3,5-Dimethyl-4-chlorophenylboronic acid</p>

CAS 1056475-86-5

3,5-DIMETHYL-4-CHLOROPHENYLBORONIC ACID

3,5-Dimethyl-4-chlorophenylboronic acid

Ref: IN-DA0090FS

3,5-Dimethyl-4-chlorophenylboronic acid

Ref: 54-OR360186

(4-Chloro-3,5-dimethylphenyl)boronic acid

Ref: 10-F219047