5-(2-Furyl)-1H-indole is an organic compound characterized by its unique structure, which combines an indole moiety with a furyl group. The indole part consists of a fused benzene and pyrrole ring, contributing to its aromatic properties and potential biological activity. The presence of the furyl group, which is a five-membered aromatic ring containing oxygen, enhances the compound's reactivity and solubility in organic solvents. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with anti-cancer or anti-inflammatory properties, as indole derivatives are known for their diverse biological activities. Additionally, the compound may participate in various chemical reactions, including electrophilic substitutions and cycloadditions, due to the electron-rich nature of the indole nitrogen and the furyl ring. Overall, 5-(2-furyl)-1H-indole is of interest in both synthetic organic chemistry and medicinal chemistry research.

5-(2-FURYL)-1H-INDOLE

128373-22-8: 5-(2-Furyl)-1H-indole is an organic compound characterized by its unique structure, which combines an indole moiety with a furyl group. The indole part consists of a fused benzene and pyrrole ring, contributing to its aromatic properties and potential biological activity. The presence of the furyl group, which is a five-membered aromatic ring containing oxygen, enhances the compound's reactivity and solubility in organic solvents. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with anti-cancer or anti-inflammatory properties, as indole derivatives are known for their diverse biological activities. Additionally, the compound may participate in various chemical reactions, including electrophilic substitutions and cycloadditions, due to the electron-rich nature of the indole nitrogen and the furyl ring. Overall, 5-(2-furyl)-1H-indole is of interest in both synthetic organic chemistry and medicinal chemistry research.

CAS 128373-22-8

5-(2-FURYL)-1H-INDOLE

5-(2-Furyl)-1H-indole

Ref: IN-DA000Y1M