3,9-Dimethoxy-6H-[1]benzofuro[3,2-c]chromen-6-one, with the CAS number 3172-99-4, is a synthetic organic compound that belongs to the class of flavonoids, specifically a chromone derivative. This compound features a complex polycyclic structure that includes a benzofuran moiety fused to a chromone ring, which contributes to its unique chemical properties. The presence of two methoxy groups at the 3 and 9 positions enhances its solubility and may influence its biological activity. Typically, compounds of this nature exhibit a range of pharmacological properties, including antioxidant, anti-inflammatory, and potential anticancer activities, making them of interest in medicinal chemistry. The compound's molecular structure allows for various interactions with biological targets, which can be explored in drug development. Additionally, its stability and reactivity can be influenced by the methoxy substituents, affecting its behavior in different chemical environments. Overall, 3,9-dimethoxy-6H-[1]benzofuro[3,2-c]chromen-6-one represents a fascinating area of study within organic and medicinal chemistry.

3,9-dimethoxy-6H-[1]benzofuro[3,2-c]chromen-6-one

3172-99-4: 3,9-Dimethoxy-6H-[1]benzofuro[3,2-c]chromen-6-one, with the CAS number 3172-99-4, is a synthetic organic compound that belongs to the class of flavonoids, specifically a chromone derivative. This compound features a complex polycyclic structure that includes a benzofuran moiety fused to a chromone ring, which contributes to its unique chemical properties. The presence of two methoxy groups at the 3 and 9 positions enhances its solubility and may influence its biological activity. Typically, compounds of this nature exhibit a range of pharmacological properties, including antioxidant, anti-inflammatory, and potential anticancer activities, making them of interest in medicinal chemistry. The compound's molecular structure allows for various interactions with biological targets, which can be explored in drug development. Additionally, its stability and reactivity can be influenced by the methoxy substituents, affecting its behavior in different chemical environments. Overall, 3,9-dimethoxy-6H-[1]benzofuro[3,2-c]chromen-6-one represents a fascinating area of study within organic and medicinal chemistry.

Coumestrol dimethylether analytical standard provided with w/w absolute assay, to be used for quantitative titration.

CAS 3172-99-4

3,9-dimethoxy-6H-[1]benzofuro[3,2-c]chromen-6-one

Coumestrol dimethylether

Ref: 11-7600S

Coumestrol dimethyl ether

Ref: 54-OR1107305

Coumestrol dimethyl ether

Ref: TR-C781005