1-Benzothiophen-5-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzothiophene moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in polar organic solvents, which makes it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. The boronic acid group is known for its ability to form reversible complexes with diols, making it valuable in applications such as drug delivery and sensor technology. Additionally, the presence of the benzothiophene structure imparts unique electronic properties, which can enhance the compound's reactivity and stability. This compound is often utilized in organic synthesis and materials science, particularly in the development of organic semiconductors and pharmaceuticals. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions during use.

1-benzothiophen-5-ylboronic acid

845872-49-3: Boronic acid, B-benzo[b]thien-5-yl-, 1-Benzothiophen-5-ylboronic acid

CAS 845872-49-3: 1-benzothiophen-5-ylboronic acid

Benzothiophene-5-boronic acid

Ref: TR-B206928

5-Benzothiopheneboronic acid

Ref: 10-F024828

5-Benzothiopheneboronic acid

Ref: 3D-VIB87249

Boronic acid,B-benzo[b]thien-5-yl-

Ref: IN-DA004UE5

Benzothiophene-5-boronic acid

Ref: 54-OR360671