4-Hydroxy-3,5-dimethoxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one, with the CAS number 2215-96-5, is an organic compound characterized by its complex structure, which includes a cyclohexadiene core with multiple functional groups. This compound features hydroxyl (-OH) and methoxy (-OCH3) groups, contributing to its reactivity and solubility in various solvents. The presence of a ketone group (2-oxopropyl) enhances its potential for undergoing nucleophilic attacks, making it a candidate for various chemical reactions, including condensation and substitution reactions. Its structural features suggest potential applications in organic synthesis and medicinal chemistry, particularly in the development of bioactive compounds. The compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Additionally, its unique arrangement of substituents may impart specific biological activities, warranting further investigation into its pharmacological properties. Overall, this compound exemplifies the intricate interplay of functional groups in organic chemistry, highlighting its potential utility in various chemical applications.

4-hydroxy-3,5-dimethoxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one

2215-96-5: 4-Hydroxy-3,5-dimethoxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one, with the CAS number 2215-96-5, is an organic compound characterized by its complex structure, which includes a cyclohexadiene core with multiple functional groups. This compound features hydroxyl (-OH) and methoxy (-OCH3) groups, contributing to its reactivity and solubility in various solvents. The presence of a ketone group (2-oxopropyl) enhances its potential for undergoing nucleophilic attacks, making it a candidate for various chemical reactions, including condensation and substitution reactions. Its structural features suggest potential applications in organic synthesis and medicinal chemistry, particularly in the development of bioactive compounds. The compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Additionally, its unique arrangement of substituents may impart specific biological activities, warranting further investigation into its pharmacological properties. Overall, this compound exemplifies the intricate interplay of functional groups in organic chemistry, highlighting its potential utility in various chemical applications.

NSC49647

<p>2,6-Dimethoxy-1-acetonylquinol: antimalarial against P. falciparum, not cytotoxic to KB cells.</p>

CAS 2215-96-5

4-hydroxy-3,5-dimethoxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one

NSC49647

Ref: IN-DA007PAT

2,6-Dimethoxy-1-acetonylquinol

Ref: TM-TN2738

2,6-Dimethoxy-1-acetonylquinol

Ref: BP-SBP00356