2-(3-Bromophenyl)-6,6-dimethyl-1-(4-(phenylcarbonyl)phenyl)-5,6,7-trihydroindol-4-one is a complex organic compound characterized by its multi-ring structure, which includes an indole moiety. The presence of bromine in the 3-position of the phenyl ring contributes to its reactivity and potential applications in medicinal chemistry. The dimethyl groups at the 6-position enhance the compound's lipophilicity, which may influence its biological activity and solubility. The phenylcarbonyl substituent at the 1-position suggests potential interactions in biological systems, possibly affecting its pharmacological properties. This compound may exhibit interesting properties such as fluorescence or photostability due to its conjugated system. Its synthesis and characterization would typically involve standard organic reactions, including bromination, acylation, and cyclization. The compound's CAS number, 1024463-73-7, allows for easy identification in chemical databases, facilitating research and development in fields such as drug discovery and materials science. Overall, this compound's unique structure positions it as a candidate for further investigation in various chemical and biological applications.

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

1024463-73-7: 2-(3-Bromophenyl)-6,6-dimethyl-1-(4-(phenylcarbonyl)phenyl)-5,6,7-trihydroindol-4-one is a complex organic compound characterized by its multi-ring structure, which includes an indole moiety. The presence of bromine in the 3-position of the phenyl ring contributes to its reactivity and potential applications in medicinal chemistry. The dimethyl groups at the 6-position enhance the compound's lipophilicity, which may influence its biological activity and solubility. The phenylcarbonyl substituent at the 1-position suggests potential interactions in biological systems, possibly affecting its pharmacological properties. This compound may exhibit interesting properties such as fluorescence or photostability due to its conjugated system. Its synthesis and characterization would typically involve standard organic reactions, including bromination, acylation, and cyclization. The compound's CAS number, 1024463-73-7, allows for easy identification in chemical databases, facilitating research and development in fields such as drug discovery and materials science. Overall, this compound's unique structure positions it as a candidate for further investigation in various chemical and biological applications.

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CAS 1024463-73-7

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

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

Ref: 3D-ZQB46373