CAS 22395-24-0
:2-(3,4-Dimethoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
Description:
2-(3,4-Dimethoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one, with the CAS number 22395-24-0, is a synthetic organic compound belonging to the class of flavonoids. This compound features a benzopyran core structure, which is characteristic of many flavonoids, and is substituted with methoxy groups that enhance its solubility and potentially its biological activity. The presence of the dimethoxyphenyl group suggests that it may exhibit interesting electronic properties and could participate in various chemical reactions. Flavonoids are known for their antioxidant properties, and this compound may also possess similar biological activities, making it of interest in pharmacological research. Its molecular structure indicates potential interactions with biological targets, which could lead to applications in medicinal chemistry. Additionally, the compound's stability, solubility, and reactivity can be influenced by the methoxy substituents, which may affect its behavior in different environments. Overall, this compound represents a fascinating area of study within the field of natural products and synthetic organic chemistry.
Formula:C18H16O5
InChI:InChI=1S/C18H16O5/c1-20-12-5-6-13-14(19)10-16(23-17(13)9-12)11-4-7-15(21-2)18(8-11)22-3/h4-10H,1-3H3
InChI key:InChIKey=VSFZYCDPDWSYSS-UHFFFAOYSA-N
SMILES:O=C1C=2C(OC(=C1)C3=CC(OC)=C(OC)C=C3)=CC(OC)=CC2
Synonyms:- 2-(3,4-Dimethoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
- 2-(3,4-Dimethoxyphenyl)-7-methoxychromen-4-one
- 2-(3,4-dimethoxyphenyl)-7-methoxy-4H-chromen-4-one
- 3′,4′,7-Trimethoxyflavone
- 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-7-methoxy-
- 7,3',4'-Trimethoxyflavone
- 7,3′,4′-Trimethoxyflavone
- Flavone, 3′,4′,7-trimethoxy-
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Found 2 products.
2-(3,4-Dimethoxyphenyl)-7-methoxy-4H-chromen-4-one
CAS:Formula:C18H16O5Color and Shape:SolidMolecular weight:312.31663',4',7-Trimethoxyflavone
CAS:<p>3',4',7-Trimethoxyflavone is a bioactive flavonoid compound, which is predominantly sourced from certain plant species, including those within the genus Kaempferia. This compound is part of the larger class of flavonoids known for their diverse biological activities. Its mode of action primarily involves modulating various cellular pathways, including signaling pathways related to inflammation, angiogenesis, and apoptosis. Recent studies suggest its potential as an inhibitor of specific enzymes and receptors, enabling its role in reducing oxidative stress and modulating immune responses.</p>Formula:C18H16O5Purity:Min. 95%Molecular weight:312.32 g/mol

