The chemical substance known as 2-{6-[(2-chlorophenyl)carbonyl]-3,4-dimethoxycyclohexa-2,4-dien-1-yl}-1-(4-methoxyphenyl)ethanone, with the CAS number 5613-32-1, is a complex organic compound characterized by its multi-functional structure. It features a cyclohexadiene core, which is substituted with various functional groups, including methoxy and carbonyl moieties. The presence of a chlorophenyl group adds to its aromatic character, potentially influencing its reactivity and interaction with biological systems. This compound may exhibit properties typical of both ketones and aromatic compounds, such as potential biological activity, including anti-inflammatory or anticancer effects, although specific biological data would need to be referenced for confirmation. Its molecular structure suggests it could participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the presence of electron-donating and electron-withdrawing groups. Overall, this compound's unique arrangement of functional groups makes it of interest in synthetic organic chemistry and medicinal chemistry research.

2-{6-[(2-chlorophenyl)carbonyl]-3,4-dimethoxycyclohexa-2,4-dien-1-yl}-1-(4-methoxyphenyl)ethanone

5613-32-1: The chemical substance known as 2-{6-[(2-chlorophenyl)carbonyl]-3,4-dimethoxycyclohexa-2,4-dien-1-yl}-1-(4-methoxyphenyl)ethanone, with the CAS number 5613-32-1, is a complex organic compound characterized by its multi-functional structure. It features a cyclohexadiene core, which is substituted with various functional groups, including methoxy and carbonyl moieties. The presence of a chlorophenyl group adds to its aromatic character, potentially influencing its reactivity and interaction with biological systems. This compound may exhibit properties typical of both ketones and aromatic compounds, such as potential biological activity, including anti-inflammatory or anticancer effects, although specific biological data would need to be referenced for confirmation. Its molecular structure suggests it could participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the presence of electron-donating and electron-withdrawing groups. Overall, this compound's unique arrangement of functional groups makes it of interest in synthetic organic chemistry and medicinal chemistry research.

CAS 5613-32-1

2-{6-[(2-chlorophenyl)carbonyl]-3,4-dimethoxycyclohexa-2,4-dien-1-yl}-1-(4-methoxyphenyl)ethanone

Methyl 4-iodo-2-methyl-3-nitrobenzoate

Ref: 54-OR20032