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6,7-Dimethoxy-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-3,4-dihydroisoquinoline is a chemical compound characterized by its complex structure, which includes an isoquinoline core substituted with methoxy and trifluoromethyl groups. The presence of two methoxy groups at the 6 and 7 positions enhances its lipophilicity and may influence its biological activity. The trifluoromethyl group, located on the phenyl ring, is known for its electron-withdrawing properties, which can significantly affect the compound's reactivity and interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in areas targeting neurological or psychiatric conditions. Additionally, the dihydroisoquinoline framework is often associated with various biological activities, including antitumor and neuroprotective effects. However, specific biological activities and mechanisms of action would require further investigation through experimental studies.

6,7-dimethoxy-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-3,4-dihydroisoquinoline

324076-69-9: 6,7-Dimethoxy-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-3,4-dihydroisoquinoline is a chemical compound characterized by its complex structure, which includes an isoquinoline core substituted with methoxy and trifluoromethyl groups. The presence of two methoxy groups at the 6 and 7 positions enhances its lipophilicity and may influence its biological activity. The trifluoromethyl group, located on the phenyl ring, is known for its electron-withdrawing properties, which can significantly affect the compound's reactivity and interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in areas targeting neurological or psychiatric conditions. Additionally, the dihydroisoquinoline framework is often associated with various biological activities, including antitumor and neuroprotective effects. However, specific biological activities and mechanisms of action would require further investigation through experimental studies.

CAS 324076-69-9

6,7-dimethoxy-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-3,4-dihydroisoquinoline

6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinoline

Ref: IN-DA007GJU