1H-Indol-7-ylboronic acid is an organic compound characterized by the presence of both an indole ring and a boronic acid functional group. The indole structure contributes to its aromatic properties, making it a planar molecule with potential for π-π stacking interactions. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, which is significant in various applications, including drug development and molecular recognition. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key building block for the formation of carbon-carbon bonds. Additionally, 1H-indol-7-ylboronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Its solubility in polar solvents and stability under standard laboratory conditions further enhance its utility in research and industrial applications. Overall, the unique combination of the indole and boronic acid functionalities positions this compound as a versatile tool in both synthetic and biological chemistry.

1H-indol-7-ylboronic acid

210889-31-9: 1H-Indol-7-ylboronic acid is an organic compound characterized by the presence of both an indole ring and a boronic acid functional group. The indole structure contributes to its aromatic properties, making it a planar molecule with potential for π-π stacking interactions. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, which is significant in various applications, including drug development and molecular recognition. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key building block for the formation of carbon-carbon bonds. Additionally, 1H-indol-7-ylboronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Its solubility in polar solvents and stability under standard laboratory conditions further enhance its utility in research and industrial applications. Overall, the unique combination of the indole and boronic acid functionalities positions this compound as a versatile tool in both synthetic and biological chemistry.

CAS 210889-31-9

1H-indol-7-ylboronic acid

Boronic acid, B-1H-indol-7-yl-

Ref: IN-DA002L1C

1H-Indole-7-boronic acid

Ref: 54-OR16982

Indole-7-boronic acid

Ref: 10-F016233