Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The specific compound "Boronic acid, [5-chloro-2-[(2,2-dimethyl-1-oxopropyl)amino]phenyl]-" (CAS 185950-64-5) features a phenyl ring substituted with a chlorine atom and an amino group linked to a dimethyl ketone moiety. This structure suggests potential reactivity in various chemical transformations, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The presence of the boronic acid functional group allows for interactions with diols, making it useful in applications such as drug development and materials science. Additionally, the chlorine substituent may influence the compound's electronic properties and reactivity, while the dimethyl-1-oxopropyl group can enhance solubility and stability. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in developing complex organic molecules.

Boronic acid, [5-chloro-2-[(2,2-dimethyl-1-oxopropyl)amino]phenyl]-

185950-64-5: Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The specific compound "Boronic acid, [5-chloro-2-[(2,2-dimethyl-1-oxopropyl)amino]phenyl]-" (CAS 185950-64-5) features a phenyl ring substituted with a chlorine atom and an amino group linked to a dimethyl ketone moiety. This structure suggests potential reactivity in various chemical transformations, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The presence of the boronic acid functional group allows for interactions with diols, making it useful in applications such as drug development and materials science. Additionally, the chlorine substituent may influence the compound's electronic properties and reactivity, while the dimethyl-1-oxopropyl group can enhance solubility and stability. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in developing complex organic molecules.

CAS 185950-64-5

Boronic acid, [5-chloro-2-[(2,2-dimethyl-1-oxopropyl)amino]phenyl]-

(5-Chloro-2-pivalamidophenyl)boronic acid

Ref: IN-DA0076BM

5-Chloro-2-(pivaloylamino)phenylboronic acid

Ref: 10-F628100