7-Hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one, also known as a flavonoid compound, exhibits several notable characteristics. This compound features a chromone backbone, which is a fused benzopyran structure, and is substituted with a hydroxyl group and a methoxyphenyl group, contributing to its potential biological activity. It is typically characterized by its yellow to orange color, which is common among flavonoids, and it may exhibit fluorescence under UV light. The presence of hydroxyl and methoxy groups enhances its solubility in organic solvents and may influence its antioxidant properties. This compound is of interest in various fields, including pharmacology and natural product chemistry, due to its potential health benefits, such as anti-inflammatory and antioxidant effects. Its molecular structure allows for interactions with biological systems, making it a candidate for further research in drug development and functional food applications. As with many flavonoids, it may also exhibit UV absorption characteristics, which can be utilized in analytical methods for its detection and quantification.

7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one

5219-16-9: 7-Hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one, also known as a flavonoid compound, exhibits several notable characteristics. This compound features a chromone backbone, which is a fused benzopyran structure, and is substituted with a hydroxyl group and a methoxyphenyl group, contributing to its potential biological activity. It is typically characterized by its yellow to orange color, which is common among flavonoids, and it may exhibit fluorescence under UV light. The presence of hydroxyl and methoxy groups enhances its solubility in organic solvents and may influence its antioxidant properties. This compound is of interest in various fields, including pharmacology and natural product chemistry, due to its potential health benefits, such as anti-inflammatory and antioxidant effects. Its molecular structure allows for interactions with biological systems, making it a candidate for further research in drug development and functional food applications. As with many flavonoids, it may also exhibit UV absorption characteristics, which can be utilized in analytical methods for its detection and quantification.

7-Hydroxy-3-(4’-methoxyphenyl)-4-methylcoumarin

CAS 5219-16-9

7-hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-chromen-2-one

7-Hydroxy-3-(4’-methoxyphenyl)-4-methylcoumarin

Ref: 54-OR351087