1-(4-(Diethylamino)phenyl)-2-(4-bromophenyl)-6-phenyl-5,6,7-trihydroindol-4-one is a complex organic compound characterized by its unique molecular structure, which includes multiple aromatic rings and a trihydroindole moiety. The presence of the diethylamino group suggests potential for enhanced solubility and biological activity, making it of interest in medicinal chemistry. The bromophenyl substituent may impart specific electronic properties, influencing the compound's reactivity and interaction with biological targets. This compound is likely to exhibit interesting photophysical properties due to its conjugated system, which could be relevant in applications such as dye-sensitized solar cells or organic light-emitting diodes. Additionally, the presence of multiple functional groups may allow for further chemical modifications, enhancing its utility in various synthetic pathways. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature, making it essential to consider these conditions in practical applications.

1-(4-(DIETHYLAMINO)PHENYL)-2-(4-BROMOPHENYL)-6-PHENYL-5,6,7-TRIHYDROINDOL-4-ONE

1024216-18-9: 1-(4-(Diethylamino)phenyl)-2-(4-bromophenyl)-6-phenyl-5,6,7-trihydroindol-4-one is a complex organic compound characterized by its unique molecular structure, which includes multiple aromatic rings and a trihydroindole moiety. The presence of the diethylamino group suggests potential for enhanced solubility and biological activity, making it of interest in medicinal chemistry. The bromophenyl substituent may impart specific electronic properties, influencing the compound's reactivity and interaction with biological targets. This compound is likely to exhibit interesting photophysical properties due to its conjugated system, which could be relevant in applications such as dye-sensitized solar cells or organic light-emitting diodes. Additionally, the presence of multiple functional groups may allow for further chemical modifications, enhancing its utility in various synthetic pathways. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature, making it essential to consider these conditions in practical applications.

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CAS 1024216-18-9

1-(4-(DIETHYLAMINO)PHENYL)-2-(4-BROMOPHENYL)-6-PHENYL-5,6,7-TRIHYDROINDOL-4-ONE

1-(4-(diethylamino)phenyl)-2-(4-bromophenyl)-6-phenyl-5,6,7-trihydroindol-4-one

Ref: 3D-ZQB21618