4-Aminophenylboronic acid is an organic compound characterized by the presence of both an amino group and a boronic acid functional group attached to a phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl ring that also carries an amino group at the para position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is attributed to its ability to form hydrogen bonds. 4-Aminophenylboronic acid is notable for its role in medicinal chemistry and materials science, particularly in the development of boron-containing compounds for drug delivery and as a building block in organic synthesis. It can participate in various chemical reactions, including Suzuki coupling, which is significant for forming carbon-carbon bonds. Additionally, the compound exhibits properties that allow it to interact with biomolecules, making it of interest in biological applications, such as in the design of sensors or therapeutic agents.

4-Aminophenylboronic acid

89415-43-0: 4-Aminophenylboronic acid is an organic compound characterized by the presence of both an amino group and a boronic acid functional group attached to a phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl ring that also carries an amino group at the para position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is attributed to its ability to form hydrogen bonds. 4-Aminophenylboronic acid is notable for its role in medicinal chemistry and materials science, particularly in the development of boron-containing compounds for drug delivery and as a building block in organic synthesis. It can participate in various chemical reactions, including Suzuki coupling, which is significant for forming carbon-carbon bonds. Additionally, the compound exhibits properties that allow it to interact with biomolecules, making it of interest in biological applications, such as in the design of sensors or therapeutic agents.

CAS 89415-43-0

4-Aminophenylboronic acid

Boronic acid,B-(4-aminophenyl)-

Ref: IN-DA0088R8

4-Aminophenylboronic acid

Ref: 7W-GK3462

4-Aminobenzeneboronic acid

Ref: 54-OR10601

4-AMINOPHENYLBORONIC ACID

Ref: 10-F466921