CAS 19202-39-2
:6-[4-(5,7-Dimethoxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy]-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
Description:
The chemical substance known as "6-[4-(5,7-Dimethoxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy]-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one," with the CAS number 19202-39-2, is a complex organic compound characterized by its polyphenolic structure. This compound features multiple methoxy groups, which enhance its solubility and may contribute to its biological activity. The presence of benzopyran moieties suggests potential antioxidant properties, as these structures are often associated with flavonoids, which are known for their health benefits. The compound's intricate arrangement of functional groups, including phenoxy and methoxy substituents, may influence its reactivity and interaction with biological targets. Additionally, the compound's molecular framework indicates potential applications in pharmaceuticals, particularly in the development of therapeutic agents due to its possible anti-inflammatory or anticancer properties. However, detailed studies on its pharmacokinetics, toxicity, and specific biological activities would be necessary to fully understand its potential uses and safety profile.
Formula:C35H28O10
InChI:InChI=1S/C35H28O10/c1-38-21-10-6-19(7-11-21)27-17-25(37)33-30(45-27)18-31(41-4)34(35(33)42-5)43-22-12-8-20(9-13-22)26-16-24(36)32-28(40-3)14-23(39-2)15-29(32)44-26/h6-18H,1-5H3
InChI key:InChIKey=XROHGCOOASGHPU-UHFFFAOYSA-N
SMILES:O(C)C1=C2C(OC(=CC2=O)C3=CC=C(OC)C=C3)=CC(OC)=C1OC4=CC=C(C=C4)C=5OC=6C(C(=O)C5)=C(OC)C=C(OC)C6
Synonyms:- Flavone, 4′,5,5′′,7,7′′-pentamethoxy-4′′′,6-oxydi-
- Hinokiflavone pentamethyl ether
- 4H-1-Benzopyran-4-one, 6-[4-(5,7-dimethoxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy]-5,7-dimethoxy-2-(4-methoxyphenyl)-
- Hinokiflavone, penta-O-methyl-
- 6-[4-(5,7-Dimethoxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy]-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
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Found 1 products.
Hinokiflavone pentamethyl ether
CAS:<p>Hinokiflavone pentamethyl ether is a synthetic flavonoid derivative, which is a chemically modified compound sourced from the natural biflavonoid, hinokiflavone. It is characterized by the methylation of phenolic hydroxyl groups, enhancing its stability and solubility. This compound can be derived through organic synthesis techniques involving the catalytic methylation of hinokiflavone.</p>Formula:C35H28O10Purity:Min. 95%Molecular weight:608.59 g/mol
