1,3-Benzothiazol-6-ylboronic acid is an organic compound characterized by the presence of a benzothiazole moiety and a boronic acid functional group. This compound typically appears as a solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group, which can form hydrogen bonds. The benzothiazole ring contributes to its aromatic properties and potential biological activity. It is often utilized in medicinal chemistry and materials science due to its ability to form complexes with various substrates, including carbohydrates and proteins, through reversible covalent bonding. The boronic acid functionality allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis. Additionally, this compound may exhibit fluorescence properties, which can be advantageous in various analytical applications. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions. Overall, 1,3-Benzothiazol-6-ylboronic acid is a versatile compound with significant implications in research and development.

1,3-Benzothiazol-6-ylboronic acid

499769-91-4: Benzo[d]thiazol-6-ylboronicacid

Benzo[d]thiazol-6-ylboronic acid

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CAS 499769-91-4: 1,3-Benzothiazol-6-ylboronic acid

1,3-Benzothiazol-6-ylboronic acid

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Benzo[d]thiazol-6-ylboronic acid

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1,3-Benzothiazol-6-ylboronic acid

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