Boronic acid, specifically B-(2-chloro-3-hydroxyphenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with a chlorine atom and a hydroxyl group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols, and having a relatively low melting point. The presence of the hydroxyl group contributes to its potential as a ligand in various chemical reactions, particularly in Suzuki coupling reactions, which are important in organic synthesis for forming carbon-carbon bonds. The chlorine substituent can influence the reactivity and stability of the compound, making it useful in medicinal chemistry and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug delivery systems. Overall, B-(2-chloro-3-hydroxyphenyl)boronic acid is a versatile compound with significant applications in synthetic organic chemistry.

Boronic acid,B-(2-chloro-3-hydroxyphenyl)-

854778-29-3: Boronic acid, specifically B-(2-chloro-3-hydroxyphenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with a chlorine atom and a hydroxyl group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols, and having a relatively low melting point. The presence of the hydroxyl group contributes to its potential as a ligand in various chemical reactions, particularly in Suzuki coupling reactions, which are important in organic synthesis for forming carbon-carbon bonds. The chlorine substituent can influence the reactivity and stability of the compound, making it useful in medicinal chemistry and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug delivery systems. Overall, B-(2-chloro-3-hydroxyphenyl)boronic acid is a versatile compound with significant applications in synthetic organic chemistry.

CAS 854778-29-3

Boronic acid,B-(2-chloro-3-hydroxyphenyl)-

Boronic acid,B-(2-chloro-3-hydroxyphenyl)-

Ref: IN-DA008F1K

(2-Chloro-3-hydroxyphenyl)boronic acid

Ref: 54-OR1054704

(2-Chloro-3-hydroxyphenyl)boronic acid

Ref: 10-F619477

(2-Chloro-3-hydroxyphenyl)boronic acid

Ref: 3D-EJB77829