Benzo[b]thiophene-3-ethanol is an organic compound characterized by its fused ring structure, which includes a benzene ring and a thiophene ring. This compound features a hydroxyl (-OH) group attached to the third position of the benzo[b]thiophene framework, contributing to its classification as an alcohol. The presence of the thiophene ring imparts unique electronic properties, making it of interest in various chemical applications, including organic electronics and pharmaceuticals. Benzo[b]thiophene-3-ethanol is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical behavior is influenced by the aromatic nature of the rings, which can participate in electrophilic substitution reactions. Additionally, the hydroxyl group can engage in hydrogen bonding, affecting its reactivity and interactions with other molecules. Overall, this compound serves as a valuable building block in synthetic organic chemistry and may have potential applications in medicinal chemistry due to its structural features.

Benzo[b]thiophene-3-ethanol

3133-87-7: Benzo[b]thiophene-3-ethanol is an organic compound characterized by its fused ring structure, which includes a benzene ring and a thiophene ring. This compound features a hydroxyl (-OH) group attached to the third position of the benzo[b]thiophene framework, contributing to its classification as an alcohol. The presence of the thiophene ring imparts unique electronic properties, making it of interest in various chemical applications, including organic electronics and pharmaceuticals. Benzo[b]thiophene-3-ethanol is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical behavior is influenced by the aromatic nature of the rings, which can participate in electrophilic substitution reactions. Additionally, the hydroxyl group can engage in hydrogen bonding, affecting its reactivity and interactions with other molecules. Overall, this compound serves as a valuable building block in synthetic organic chemistry and may have potential applications in medicinal chemistry due to its structural features.

CAS 3133-87-7

Benzo[b]thiophene-3-ethanol

2-(1-Benzothiophen-3-yl)ethan-1-ol

Ref: 3D-DAA13387