The chemical substance known as 2-phenylethyl 4-[4-(benzyloxy)-3-methoxyphenyl]-7-(4-chlorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate, with the CAS number 5706-14-9, is a complex organic compound characterized by its multi-ring structure and various functional groups. It features a hexahydroquinoline core, which is a bicyclic structure known for its presence in various bioactive compounds. The presence of a carboxylate group suggests potential acidic properties, while the methoxy and benzyloxy substituents indicate the compound may exhibit interesting electronic and steric effects, potentially influencing its reactivity and solubility. The chlorophenyl group adds to the compound's complexity and may enhance its biological activity. Overall, this compound is likely to be of interest in medicinal chemistry and pharmacology due to its structural diversity, which may correlate with various biological activities. However, specific properties such as solubility, melting point, and biological activity would require empirical investigation for detailed characterization.

2-phenylethyl 4-[4-(benzyloxy)-3-methoxyphenyl]-7-(4-chlorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

5706-14-9: The chemical substance known as 2-phenylethyl 4-[4-(benzyloxy)-3-methoxyphenyl]-7-(4-chlorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate, with the CAS number 5706-14-9, is a complex organic compound characterized by its multi-ring structure and various functional groups. It features a hexahydroquinoline core, which is a bicyclic structure known for its presence in various bioactive compounds. The presence of a carboxylate group suggests potential acidic properties, while the methoxy and benzyloxy substituents indicate the compound may exhibit interesting electronic and steric effects, potentially influencing its reactivity and solubility. The chlorophenyl group adds to the compound's complexity and may enhance its biological activity. Overall, this compound is likely to be of interest in medicinal chemistry and pharmacology due to its structural diversity, which may correlate with various biological activities. However, specific properties such as solubility, melting point, and biological activity would require empirical investigation for detailed characterization.

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CAS 5706-14-9

2-phenylethyl 4-[4-(benzyloxy)-3-methoxyphenyl]-7-(4-chlorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

2-((4-Methoxyphenyl)methylene)indan-1-one

Ref: 3D-FM169763