(5-Boronobenzofuran-2-yl)boronic acid is an organoboron compound characterized by the presence of both boronic acid and benzofuran moieties. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid functional group. The boron atoms in the structure can participate in various chemical reactions, making it useful in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The benzofuran ring contributes to its aromatic properties, which can influence its reactivity and interactions with biological targets. Additionally, this compound may exhibit unique optical properties due to its conjugated system, making it of interest in materials science and sensor applications. Its reactivity as a boronic acid allows for the formation of covalent bonds with diols, which is a key feature in the development of drug delivery systems and in the synthesis of complex organic molecules. Overall, (5-boronobenzofuran-2-yl)boronic acid is a versatile compound with significant potential in various fields of chemistry.

(5-boronobenzofuran-2-yl)boronic acid

913835-69-5: (5-Boronobenzofuran-2-yl)boronic acid is an organoboron compound characterized by the presence of both boronic acid and benzofuran moieties. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid functional group. The boron atoms in the structure can participate in various chemical reactions, making it useful in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The benzofuran ring contributes to its aromatic properties, which can influence its reactivity and interactions with biological targets. Additionally, this compound may exhibit unique optical properties due to its conjugated system, making it of interest in materials science and sensor applications. Its reactivity as a boronic acid allows for the formation of covalent bonds with diols, which is a key feature in the development of drug delivery systems and in the synthesis of complex organic molecules. Overall, (5-boronobenzofuran-2-yl)boronic acid is a versatile compound with significant potential in various fields of chemistry.

CAS 913835-69-5

(5-boronobenzofuran-2-yl)boronic acid

Benzofuran-2,5-diboronic acid

Ref: IN-DA003O23

Benzofuran-2,5-yldiboronic acid

Ref: 54-OR3323