5-Iodo-2-indanone is an organic compound characterized by its indanone structure, which consists of a fused benzene and cyclopentanone ring system. The presence of an iodine atom at the 5-position of the indanone ring significantly influences its chemical properties, including reactivity and polarity. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water due to its hydrophobic nature. The iodine substituent can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Additionally, 5-Iodo-2-indanone may exhibit biological activity, which can be explored for potential applications in pharmaceuticals or agrochemicals. Its molecular structure and functional groups contribute to its unique reactivity profile, making it of interest in both academic research and industrial applications. Safety precautions should be observed when handling this compound, as iodine-containing substances can pose health risks.

5-Iodo-2-indanone

1187983-92-1: 5-Iodo-2-indanone is an organic compound characterized by its indanone structure, which consists of a fused benzene and cyclopentanone ring system. The presence of an iodine atom at the 5-position of the indanone ring significantly influences its chemical properties, including reactivity and polarity. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water due to its hydrophobic nature. The iodine substituent can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Additionally, 5-Iodo-2-indanone may exhibit biological activity, which can be explored for potential applications in pharmaceuticals or agrochemicals. Its molecular structure and functional groups contribute to its unique reactivity profile, making it of interest in both academic research and industrial applications. Safety precautions should be observed when handling this compound, as iodine-containing substances can pose health risks.

CAS 1187983-92-1

5-Iodo-2-indanone

5-Iodo-1H-inden-2(3H)-one

Ref: IN-DA008UDX