CAS 14348-21-1
:7H-Furo[3,2-g][1]benzopyran-7-one,4,9-bis[(3-methyl-2-buten-1-yl)oxy]-
Description:
7H-Furo[3,2-g][1]benzopyran-7-one, 4,9-bis[(3-methyl-2-buten-1-yl)oxy]- is a complex organic compound characterized by its fused furobenzopyran structure, which incorporates both a furan and a benzopyran moiety. This compound features multiple functional groups, including ether linkages due to the presence of bis[(3-methyl-2-buten-1-yl)oxy] substituents, which contribute to its reactivity and potential biological activity. The presence of the 3-methyl-2-buten-1-yl groups suggests that it may exhibit properties typical of terpenoids, potentially influencing its solubility and interaction with biological systems. The compound's structure indicates it may participate in various chemical reactions, including those typical of phenolic compounds, such as oxidation or substitution reactions. Its unique arrangement of atoms and functional groups may also impart specific optical properties, making it of interest in fields such as medicinal chemistry and materials science. Overall, this compound's intricate structure and functional diversity suggest potential applications in pharmaceuticals or as a natural product derivative.
Formula:C21H22O5
Synonyms:- 7H-Furo[3,2-g][1]benzopyran-7-one,4,9-bis[(3-methyl-2-butenyl)oxy]- (8CI,9CI)
- Cnidicin
- 7H-Furo[3,2-g][1]benzopyran-7-one,4,9-bis[(3-methyl-2-buten-1-yl)oxy]-
- 4,9-Bis[(3-methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one
- 4,9-Bis((3-methylbut-2-en-1-yl)oxy)-7H-furo[3,2-g]chromen-7-one
- kinidilin
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Found 6 products.
4,9-Bis[(3-methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one
CAS:Formula:C21H22O5Purity:98%Molecular weight:354.3964Cnidicin
CAS:<p>Cnidicin: anti-allergic, anti-inflammatory, impedes mast cell degranulation, NO in RAW 264.7 cells (IC50=7.5µM), hinders human tumor cell growth in vitro.</p>Formula:C21H22O5Purity:99.16% - 99.49%Color and Shape:SolidMolecular weight:354.4Cnidicin
CAS:<p>Cnidicin is a bioactive compound, which is a natural product extracted from Cnidium plants. It is primarily obtained from species such as Cnidium monnieri, commonly found in traditional Chinese medicine. The mode of action of Cnidicin involves modulation of various cellular pathways, potentially influencing enzyme activities and receptor interactions. This compound is known for its antioxidant, anti-inflammatory, and antimicrobial properties, making it a valuable subject of research in the field of pharmacology.</p>Formula:C21H22O5Purity:Min. 95%Molecular weight:354.4 g/mol






