3-(4-Methoxyphenyl)-2H-chromen-2-one, also known as a flavonoid derivative, is characterized by its chromone backbone, which consists of a benzopyran structure. This compound features a methoxy group attached to a phenyl ring at the 4-position, contributing to its unique chemical properties and potential biological activities. It typically exhibits a yellow to orange color, indicative of its conjugated double bond system, which can absorb light in the UV-visible spectrum. The presence of the methoxy group enhances its lipophilicity, potentially influencing its solubility and interaction with biological membranes. This compound may possess antioxidant, anti-inflammatory, and anticancer properties, making it of interest in pharmaceutical and nutraceutical research. Its structural features allow for various chemical modifications, which can lead to the development of derivatives with enhanced efficacy or selectivity. As with many flavonoids, it may also exhibit a range of biological activities, including enzyme inhibition and modulation of cell signaling pathways.

3-(4-methoxyphenyl)-2H-chromen-2-one

23000-33-1: 3-(4-Methoxyphenyl)-2H-chromen-2-one, also known as a flavonoid derivative, is characterized by its chromone backbone, which consists of a benzopyran structure. This compound features a methoxy group attached to a phenyl ring at the 4-position, contributing to its unique chemical properties and potential biological activities. It typically exhibits a yellow to orange color, indicative of its conjugated double bond system, which can absorb light in the UV-visible spectrum. The presence of the methoxy group enhances its lipophilicity, potentially influencing its solubility and interaction with biological membranes. This compound may possess antioxidant, anti-inflammatory, and anticancer properties, making it of interest in pharmaceutical and nutraceutical research. Its structural features allow for various chemical modifications, which can lead to the development of derivatives with enhanced efficacy or selectivity. As with many flavonoids, it may also exhibit a range of biological activities, including enzyme inhibition and modulation of cell signaling pathways.

CAS 23000-33-1

3-(4-methoxyphenyl)-2H-chromen-2-one

2H-1-Benzopyran-2-one, 3-(4-methoxyphenyl)-

Ref: IN-DA002LTC

3-(4'-Methoxyphenyl)coumarin

Ref: 54-OR351298