Boronic acid, specifically 2,3-dichloro-4-methylphenyl boronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a substituted aromatic ring. The compound features a dichlorinated phenyl group, which enhances its reactivity and solubility in various organic solvents. The presence of the methyl group contributes to its steric properties, influencing its interactions in chemical reactions. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis, particularly in the formation of boronate esters. This compound may also exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its unique structural features allow for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the synthesis of complex organic molecules. Overall, 2,3-dichloro-4-methylphenyl boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

Boronic acid,(2,3-dichloro-4-methylphenyl)- (9CI)

352535-95-6: Boronic acid, specifically 2,3-dichloro-4-methylphenyl boronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a substituted aromatic ring. The compound features a dichlorinated phenyl group, which enhances its reactivity and solubility in various organic solvents. The presence of the methyl group contributes to its steric properties, influencing its interactions in chemical reactions. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis, particularly in the formation of boronate esters. This compound may also exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its unique structural features allow for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the synthesis of complex organic molecules. Overall, 2,3-dichloro-4-methylphenyl boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

CAS 352535-95-6

Boronic acid,(2,3-dichloro-4-methylphenyl)- (9CI)

2,3-Dichloro-4-methylphenylboronic acid

Ref: IN-DA00CTB3

2,3-Dichloro-4-methylphenylboronic acid

Ref: 10-F627531