Boronic acid, specifically the compound known as [2-[(dimethylamino)methyl]-5-methoxyphenyl]-, dimethylester, is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a methoxy group that enhances its solubility and reactivity, as well as a dimethylamino group that can influence its electronic properties and reactivity. The presence of these functional groups suggests that the compound may exhibit interesting properties in organic synthesis, particularly in cross-coupling reactions and as a building block in the development of pharmaceuticals. Additionally, boronic acids are often utilized in the formation of boronate esters, which are important in various chemical transformations. The compound's structure allows for potential applications in medicinal chemistry, particularly in the design of inhibitors or modulators of biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic organic chemistry.

Boronic acid, [2-[(dimethylamino)methyl]-5-methoxyphenyl]-, dimethylester

89291-27-0: Boronic acid, specifically the compound known as [2-[(dimethylamino)methyl]-5-methoxyphenyl]-, dimethylester, is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a methoxy group that enhances its solubility and reactivity, as well as a dimethylamino group that can influence its electronic properties and reactivity. The presence of these functional groups suggests that the compound may exhibit interesting properties in organic synthesis, particularly in cross-coupling reactions and as a building block in the development of pharmaceuticals. Additionally, boronic acids are often utilized in the formation of boronate esters, which are important in various chemical transformations. The compound's structure allows for potential applications in medicinal chemistry, particularly in the design of inhibitors or modulators of biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic organic chemistry.

CAS 89291-27-0

Boronic acid, [2-[(dimethylamino)methyl]-5-methoxyphenyl]-, dimethylester

Boronic acid, [2-[(dimethylamino)methyl]-5-methoxyphenyl]-, dimethylester

Ref: IN-DAN-PC-0VOSOA