3-(4-Bromophenyl)-5-(hydroxyimino)-7-(2-methylpropyl)-6,7,8-trihydrocinnoline is a complex organic compound characterized by its unique structural features, including a trihydrocinnoline core, a bromophenyl substituent, and a hydroxyimino group. The presence of the bromine atom introduces significant electronegativity, which can influence the compound's reactivity and interaction with biological systems. The hydroxyimino functional group contributes to the compound's potential as a ligand in coordination chemistry or as a precursor in organic synthesis. Additionally, the branched alkyl group (2-methylpropyl) may enhance lipophilicity, affecting the compound's solubility and permeability in biological membranes. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its specific applications and biological activities would depend on detailed studies, including structure-activity relationship analyses. Overall, the compound's unique features suggest potential utility in various chemical and pharmaceutical contexts.

3-(4-BROMOPHENYL)-5-(HYDROXYIMINO)-7-(2-METHYLPROPYL)-6,7,8-TRIHYDROCINNOLINE

1274947-99-7: 3-(4-Bromophenyl)-5-(hydroxyimino)-7-(2-methylpropyl)-6,7,8-trihydrocinnoline is a complex organic compound characterized by its unique structural features, including a trihydrocinnoline core, a bromophenyl substituent, and a hydroxyimino group. The presence of the bromine atom introduces significant electronegativity, which can influence the compound's reactivity and interaction with biological systems. The hydroxyimino functional group contributes to the compound's potential as a ligand in coordination chemistry or as a precursor in organic synthesis. Additionally, the branched alkyl group (2-methylpropyl) may enhance lipophilicity, affecting the compound's solubility and permeability in biological membranes. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its specific applications and biological activities would depend on detailed studies, including structure-activity relationship analyses. Overall, the compound's unique features suggest potential utility in various chemical and pharmaceutical contexts.

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CAS 1274947-99-7

3-(4-BROMOPHENYL)-5-(HYDROXYIMINO)-7-(2-METHYLPROPYL)-6,7,8-TRIHYDROCINNOLINE

3-(4-bromophenyl)-5-(hydroxyimino)-7-(2-methylpropyl)-6,7,8-trihydrocinnoline

Ref: 3D-ZAC94799