7-Hydroxy-4-methyl-3-prop-2-en-1-yl-2H-chromen-2-one, also known as a derivative of flavonoids, exhibits several notable characteristics. This compound features a chromone backbone, which is a bicyclic structure consisting of a benzene ring fused to a pyrone ring. The presence of the hydroxy group at the 7-position contributes to its potential antioxidant properties, while the 4-methyl and prop-2-en-1-yl substituents enhance its reactivity and biological activity. This compound is typically characterized by its ability to absorb ultraviolet light, which is common among flavonoids, and it may exhibit various biological activities, including anti-inflammatory and antimicrobial effects. Its solubility can vary depending on the solvent, and it may be more soluble in organic solvents than in water. The compound's structure suggests potential applications in pharmaceuticals, cosmetics, and food industries, particularly due to its bioactive properties. As with many flavonoids, further research is necessary to fully elucidate its mechanisms of action and potential therapeutic uses.

7-hydroxy-4-methyl-3-prop-2-en-1-yl-2H-chromen-2-one

26481-13-0: 7-Hydroxy-4-methyl-3-prop-2-en-1-yl-2H-chromen-2-one, also known as a derivative of flavonoids, exhibits several notable characteristics. This compound features a chromone backbone, which is a bicyclic structure consisting of a benzene ring fused to a pyrone ring. The presence of the hydroxy group at the 7-position contributes to its potential antioxidant properties, while the 4-methyl and prop-2-en-1-yl substituents enhance its reactivity and biological activity. This compound is typically characterized by its ability to absorb ultraviolet light, which is common among flavonoids, and it may exhibit various biological activities, including anti-inflammatory and antimicrobial effects. Its solubility can vary depending on the solvent, and it may be more soluble in organic solvents than in water. The compound's structure suggests potential applications in pharmaceuticals, cosmetics, and food industries, particularly due to its bioactive properties. As with many flavonoids, further research is necessary to fully elucidate its mechanisms of action and potential therapeutic uses.

CAS 26481-13-0

7-hydroxy-4-methyl-3-prop-2-en-1-yl-2H-chromen-2-one

3-Allyl-7-hydroxy-4-methyl-2H-chromen-2-one

Ref: IN-DA002TEA

3-allyl-7-hydroxy-4-methyl-2H-chromen-2-one

Ref: 10-F313945