CAS 17245-30-6
:4H-1-Benzopyran-4-one,3,5,6,7-tetramethoxy-2-(3,4,5-trimethoxyphenyl)-
Description:
4H-1-Benzopyran-4-one, 3,5,6,7-tetramethoxy-2-(3,4,5-trimethoxyphenyl)-, commonly referred to by its CAS number 17245-30-6, 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 multiple methoxy groups that enhance its solubility and potentially its biological activity. The presence of these methoxy groups can influence the compound's electronic properties, making it a subject of interest in various fields, including medicinal chemistry and natural product research. The compound may exhibit antioxidant, anti-inflammatory, or other pharmacological activities, although specific biological effects would depend on further empirical studies. Its complex structure suggests potential applications in pharmaceuticals, particularly in the development of therapeutic agents. As with many organic compounds, its stability, reactivity, and interactions with other substances would be influenced by its molecular structure and functional groups.
Formula:C22H24O9
Synonyms:- Flavone,3,3',4',5,5',6,7-heptamethoxy- (7CI,8CI)
- 3,3',4',5,5',6,7-Heptamethoxyflavone
- 3,5,6,7,3',4',5'-Heptamethoxyflavone
- 3',4',5',3,5,6,7-Heptamethoxyflavone
- Nsc684433
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Found 4 products.
3',4',5',3,5,6,7-Heptamethoxyflavone
CAS:<p>3',4',5',3,5,6,7-Heptamethoxyflavone is a natural product for research related to life sciences. The catalog number is TN2864 and the CAS number is 17245-30-6.</p>Formula:C22H24O9Purity:98%Color and Shape:SolidMolecular weight:432.423',4',5',3,5,6,7-Heptamethoxyflavone
CAS:Formula:C22H24O9Purity:95%~99%Color and Shape:Yellow cryst.Molecular weight:432.4253',4',5',3,5,6,7-Heptamethoxyflavone
CAS:<p>3',4',5',3,5,6,7-Heptamethoxyflavone is a naturally occurring flavonoid, which is primarily found in citrus fruits. As an O-methylated flavone, it is characterized by the presence of methoxy groups attached to its flavonoid backbone. Its mode of action involves modulating multiple signaling pathways, which include the inhibition of various enzyme activities and the modulation of transcription factors. These actions contribute to its well-documented antioxidant and anti-inflammatory activities.</p>Formula:C22H24O9Purity:Min. 95%Molecular weight:432.4 g/mol




