1-(3,4-Difluorophenyl)-2,6-dimethyl-5,6,7-trihydroindol-4-one is a chemical compound characterized by its complex structure, which includes an indole core substituted with a difluorophenyl group and additional methyl groups. This compound typically exhibits properties associated with indole derivatives, such as potential biological activity, including anti-inflammatory or anticancer effects, although specific biological data may vary. The presence of fluorine atoms can enhance lipophilicity and influence the compound's interaction with biological targets. The molecular structure suggests that it may participate in various chemical reactions, including electrophilic aromatic substitution due to the electron-withdrawing nature of the fluorine substituents. Additionally, the compound's solubility, stability, and reactivity can be influenced by the presence of the methyl groups and the overall steric hindrance. As with many organic compounds, its physical properties, such as melting point and boiling point, would need to be determined experimentally. Overall, this compound represents a class of molecules that may have significant implications in medicinal chemistry and drug development.

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

1023536-44-8: 1-(3,4-Difluorophenyl)-2,6-dimethyl-5,6,7-trihydroindol-4-one is a chemical compound characterized by its complex structure, which includes an indole core substituted with a difluorophenyl group and additional methyl groups. This compound typically exhibits properties associated with indole derivatives, such as potential biological activity, including anti-inflammatory or anticancer effects, although specific biological data may vary. The presence of fluorine atoms can enhance lipophilicity and influence the compound's interaction with biological targets. The molecular structure suggests that it may participate in various chemical reactions, including electrophilic aromatic substitution due to the electron-withdrawing nature of the fluorine substituents. Additionally, the compound's solubility, stability, and reactivity can be influenced by the presence of the methyl groups and the overall steric hindrance. As with many organic compounds, its physical properties, such as melting point and boiling point, would need to be determined experimentally. Overall, this compound represents a class of molecules that may have significant implications in medicinal chemistry and drug development.

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CAS 1023536-44-8

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

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

Ref: 3D-YQB53644