Boronic acid, specifically the compound with the name "2-[[methyl(phenylmethyl)amino]methyl]phenyl]-" and CAS number 209396-01-0, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a methyl(phenylmethyl)amino group. This structure imparts unique properties, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic phenyl groups. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the amino group can enhance reactivity and facilitate interactions with biological molecules, potentially leading to applications in drug development and materials science. Overall, this compound exemplifies the versatility of boronic acids in both synthetic and applied chemistry.

Boronic acid, [2-[[methyl(phenylmethyl)amino]methyl]phenyl]-

209396-01-0: Boronic acid, specifically the compound with the name "2-[[methyl(phenylmethyl)amino]methyl]phenyl]-" and CAS number 209396-01-0, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a methyl(phenylmethyl)amino group. This structure imparts unique properties, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic phenyl groups. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the amino group can enhance reactivity and facilitate interactions with biological molecules, potentially leading to applications in drug development and materials science. Overall, this compound exemplifies the versatility of boronic acids in both synthetic and applied chemistry.

CAS 209396-01-0

Boronic acid, [2-[[methyl(phenylmethyl)amino]methyl]phenyl]-

(2-((benzyl(methyl)amino)methyl)phenyl)boronic acid

Ref: IN-DA01FNNG