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1 References  













Spinacetin






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From Wikipedia, the free encyclopedia
  

Spinacetin
Chemical structure of spinacetin
Names
IUPAC name

3,4′,5,7-Tetrahydroxy-3′,6′-dimethoxyflavone

Systematic IUPAC name

3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-4H-1-benzopyran-4-one

Other names

Quercetagetin 3',6-dimethyl ether

Identifiers

CAS Number

3D model (JSmol)
ChemSpider

PubChem CID
UNII

CompTox Dashboard (EPA)

  • InChI=1S/C17H14O8/c1-23-10-5-7(3-4-8(10)18)16-15(22)13(20)12-11(25-16)6-9(19)17(24-2)14(12)21/h3-6,18-19,21-22H,1-2H3 ☒N

    Key: XWIDINOKCRFVHQ-UHFFFAOYSA-N ☒N

  • InChI=1/C17H14O8/c1-23-10-5-7(3-4-8(10)18)16-15(22)13(20)12-11(25-16)6-9(19)17(24-2)14(12)21/h3-6,18-19,21-22H,1-2H3

    Key: XWIDINOKCRFVHQ-UHFFFAOYAE

  • COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)O)OC)O)O)O

Properties

Chemical formula

 C17H14O8
Molar mass 346.291 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Spinacetin is an O-methylated flavonol. It can be found in spinach (Spinacia oleracea).[1]

References[edit]

  1. ^ Aehle, Elke; Raynaud-Le Grandic, Sophie; Ralainirina, Robert; Baltora-Rosset, Sylvie; Mesnard, François; Prouillet, Christophe; Mazière, Jean-Claude; Fliniaux, Marc-André (2004). "Development and evaluation of an enriched natural antioxidant preparation obtained from aqueous spinach (Spinacia oleracea) extracts by an adsorption procedure". Food Chemistry. 86 (4): 579–585. doi:10.1016/j.foodchem.2003.10.006.


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    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Spinacetin&oldid=1153564331"
    Categories: 
    ●O-methylated flavonols
     ●Resorcinols
     ●Aromatic compound stubs
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