(4-((Diisopropylamino)methyl)phenyl)boronic acid 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 phenyl ring substituted with a diisopropylamino group and a boronic acid moiety, contributing to its potential applications in medicinal chemistry and materials science. The diisopropylamino group enhances solubility and can influence the compound's reactivity and biological activity. Boronic acids are often utilized in Suzuki coupling reactions, making this compound valuable in organic synthesis. Additionally, the presence of the amino group may impart basic properties, allowing for interactions with various biological targets. The compound's structure suggests it may exhibit interesting properties such as fluorescence or catalytic activity, depending on the specific conditions and environments in which it is used. Overall, (4-((diisopropylamino)methyl)phenyl)boronic acid is a versatile compound with significant potential in various chemical applications.

(4-((diisopropylaMino)Methyl)phenyl)boronic acid

1025900-35-9: (4-((Diisopropylamino)methyl)phenyl)boronic acid 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 phenyl ring substituted with a diisopropylamino group and a boronic acid moiety, contributing to its potential applications in medicinal chemistry and materials science. The diisopropylamino group enhances solubility and can influence the compound's reactivity and biological activity. Boronic acids are often utilized in Suzuki coupling reactions, making this compound valuable in organic synthesis. Additionally, the presence of the amino group may impart basic properties, allowing for interactions with various biological targets. The compound's structure suggests it may exhibit interesting properties such as fluorescence or catalytic activity, depending on the specific conditions and environments in which it is used. Overall, (4-((diisopropylamino)methyl)phenyl)boronic acid is a versatile compound with significant potential in various chemical applications.

CAS 1025900-35-9

(4-((diisopropylaMino)Methyl)phenyl)boronic acid

(4-((Diisopropylamino)methyl)phenyl)boronic acid

Ref: IN-DA0095HU