7-Methyl-5-(1-methyl-2-oxopropoxy)-4-propyl-2H-chromen-2-one, identified by its CAS number 314742-59-1, is a synthetic organic compound belonging to the class of flavonoids, specifically a chromenone derivative. This compound features a chromone backbone, characterized by a benzopyran structure, which is known for its diverse biological activities. The presence of the methyl and propyl groups contributes to its hydrophobic properties, potentially influencing its solubility and interaction with biological membranes. The oxopropoxy substituent may enhance its reactivity and biological activity, possibly affecting its pharmacological profile. Compounds of this nature are often studied for their potential antioxidant, anti-inflammatory, and anticancer properties. Additionally, the structural modifications can lead to variations in their biological efficacy and selectivity. As with many flavonoids, the compound may exhibit a range of interactions with enzymes and receptors, making it a subject of interest in medicinal chemistry and drug development. Further research is necessary to fully elucidate its properties and potential applications.

7-methyl-5-(1-methyl-2-oxopropoxy)-4-propyl-2H-chromen-2-one

314742-59-1: 7-Methyl-5-(1-methyl-2-oxopropoxy)-4-propyl-2H-chromen-2-one, identified by its CAS number 314742-59-1, is a synthetic organic compound belonging to the class of flavonoids, specifically a chromenone derivative. This compound features a chromone backbone, characterized by a benzopyran structure, which is known for its diverse biological activities. The presence of the methyl and propyl groups contributes to its hydrophobic properties, potentially influencing its solubility and interaction with biological membranes. The oxopropoxy substituent may enhance its reactivity and biological activity, possibly affecting its pharmacological profile. Compounds of this nature are often studied for their potential antioxidant, anti-inflammatory, and anticancer properties. Additionally, the structural modifications can lead to variations in their biological efficacy and selectivity. As with many flavonoids, the compound may exhibit a range of interactions with enzymes and receptors, making it a subject of interest in medicinal chemistry and drug development. Further research is necessary to fully elucidate its properties and potential applications.

CAS 314742-59-1

7-methyl-5-(1-methyl-2-oxopropoxy)-4-propyl-2H-chromen-2-one

7-Methyl-5-(1-methyl-2-oxopropoxy)-4-propyl-2h-chromen-2-one

Ref: IN-DA00C64K

7-methyl-5-(1-methyl-2-oxopropoxy)-4-propyl-2H-chromen-2-one

Ref: 10-F314861