1-(3,5-Difluorophenyl)-2-(3-bromophenyl)-6,6-dimethyl-5,6,7-trihydroindol-4-one is a synthetic organic compound characterized by its complex structure, which includes multiple aromatic rings and halogen substituents. The presence of difluoro and bromo groups suggests that this compound may exhibit unique electronic properties, potentially influencing its reactivity and interactions with biological targets. The trihydroindole core structure is indicative of potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. This compound may possess interesting pharmacological activities due to its structural features, which can affect its solubility, stability, and binding affinity to various biological molecules. Additionally, the presence of dimethyl groups can enhance lipophilicity, potentially improving bioavailability. As with many synthetic compounds, the specific characteristics such as melting point, solubility, and spectral properties would need to be determined experimentally. Overall, this compound represents a class of indole derivatives that may be of interest in drug discovery and development.

1-(3,5-DIFLUOROPHENYL)-2-(3-BROMOPHENYL)-6,6-DIMETHYL-5,6,7-TRIHYDROINDOL-4-ONE

1024154-45-7: 1-(3,5-Difluorophenyl)-2-(3-bromophenyl)-6,6-dimethyl-5,6,7-trihydroindol-4-one is a synthetic organic compound characterized by its complex structure, which includes multiple aromatic rings and halogen substituents. The presence of difluoro and bromo groups suggests that this compound may exhibit unique electronic properties, potentially influencing its reactivity and interactions with biological targets. The trihydroindole core structure is indicative of potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. This compound may possess interesting pharmacological activities due to its structural features, which can affect its solubility, stability, and binding affinity to various biological molecules. Additionally, the presence of dimethyl groups can enhance lipophilicity, potentially improving bioavailability. As with many synthetic compounds, the specific characteristics such as melting point, solubility, and spectral properties would need to be determined experimentally. Overall, this compound represents a class of indole derivatives that may be of interest in drug discovery and development.

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CAS 1024154-45-7

1-(3,5-DIFLUOROPHENYL)-2-(3-BROMOPHENYL)-6,6-DIMETHYL-5,6,7-TRIHYDROINDOL-4-ONE

1-(3,5-difluorophenyl)-2-(3-bromophenyl)-6,6-dimethyl-5,6,7-trihydroindol-4-one

Ref: 3D-ZQB15445