CAS 86548-40-5
:5,7-dimethoxy-3-(naphthalen-1-ylcarbonyl)-2H-chromen-2-one
Description:
5,7-Dimethoxy-3-(naphthalen-1-ylcarbonyl)-2H-chromen-2-one, with the CAS number 86548-40-5, is a synthetic organic compound belonging to the class of flavonoids, specifically a chromone derivative. This compound features a chromone backbone, characterized by a benzopyran structure, which is substituted at the 5 and 7 positions with methoxy groups, enhancing its solubility and potential biological activity. The presence of a naphthalen-1-ylcarbonyl group at the 3 position contributes to its structural complexity and may influence its pharmacological properties. Generally, compounds of this type are studied for their potential antioxidant, anti-inflammatory, and anticancer activities due to the presence of the flavonoid structure, which is known for its ability to scavenge free radicals. The specific characteristics, such as melting point, solubility, and spectral data, would typically be determined through experimental methods and can vary based on purity and environmental conditions. Overall, this compound represents a fascinating area of research in medicinal chemistry and natural product synthesis.
Formula:C22H16O5
InChI:InChI=1/C22H16O5/c1-25-14-10-19(26-2)17-12-18(22(24)27-20(17)11-14)21(23)16-9-5-7-13-6-3-4-8-15(13)16/h3-12H,1-2H3
SMILES:COc1cc(c2cc(C(=O)c3cccc4ccccc34)c(=O)oc2c1)OC
Synonyms:- 2H-1-benzopyran-2-one, 5,7-dimethoxy-3-(1-naphthalenylcarbonyl)-
- 5,7-Dimethoxy-3-(1-naphthoyl)-2H-chromen-2-one
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Found 2 products.
5,7-Dimethoxy-3-(1-naphthoyl)coumarin
CAS:Controlled Product<p>Applications Coumarin derivatives are involved in photogeneration of reactive oxygen species from ketocoumarins.<br>References McCord, J., et al.: J. Biol. Chem., 244, 6049 (1969), Peters, G., et al.: Biochim. Biophys. Acta, 637, 43 (1981), Reszka, K., et al.: J. Photochem. Photobiol., 55, 359 (1992), Lee, M., et al.: J. Med. Chem., 37, 1208 (1994),<br></p>Formula:C22H16O5Color and Shape:NeatMolecular weight:360.36

