3-(4-Bromophenyl)-7-methyl-2,6,7,8,4A-pentahydrocinnolin-5-one is a chemical compound characterized by its complex bicyclic structure, which includes a pentahydrocinnoline core. The presence of a bromophenyl group indicates that it has a bromine atom substituted on a phenyl ring, which can influence its reactivity and biological activity. The methyl group at the 7-position contributes to the compound's overall hydrophobic character. This compound may exhibit interesting pharmacological properties due to its structural features, potentially interacting with various biological targets. Its molecular structure suggests it could participate in hydrogen bonding and hydrophobic interactions, which are crucial for its solubility and bioavailability. The compound's CAS number, 1024074-57-4, allows for precise identification in chemical databases, facilitating research and application in fields such as medicinal chemistry and drug development. As with many organic compounds, its stability, reactivity, and potential applications would depend on the specific conditions under which it is studied or utilized.

3-(4-BROMOPHENYL)-7-METHYL-2,6,7,8,4A-PENTAHYDROCINNOLIN-5-ONE

1024074-57-4: 3-(4-Bromophenyl)-7-methyl-2,6,7,8,4A-pentahydrocinnolin-5-one is a chemical compound characterized by its complex bicyclic structure, which includes a pentahydrocinnoline core. The presence of a bromophenyl group indicates that it has a bromine atom substituted on a phenyl ring, which can influence its reactivity and biological activity. The methyl group at the 7-position contributes to the compound's overall hydrophobic character. This compound may exhibit interesting pharmacological properties due to its structural features, potentially interacting with various biological targets. Its molecular structure suggests it could participate in hydrogen bonding and hydrophobic interactions, which are crucial for its solubility and bioavailability. The compound's CAS number, 1024074-57-4, allows for precise identification in chemical databases, facilitating research and application in fields such as medicinal chemistry and drug development. As with many organic compounds, its stability, reactivity, and potential applications would depend on the specific conditions under which it is studied or utilized.

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CAS 1024074-57-4

3-(4-BROMOPHENYL)-7-METHYL-2,6,7,8,4A-PENTAHYDROCINNOLIN-5-ONE

3-(4-bromophenyl)-7-methyl-2,6,7,8,4a-pentahydrocinnolin-5-one

Ref: 3D-ZQB07457