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Pseudobaptigenin

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Pseudobaptigenin
Chemical structure of pseudobaptigenin
Pseudobaptigenin molecule
Names
IUPAC name 7-Hydroxy-3′,4′-isoflavone
Systematic IUPAC name 3-(2H-1,3-Benzodioxol-5-yl)-7-hydroxy-4H-1-benzopyran-4-one
Other names ψ-Baptigenin
Psi-baptigenin
7-Hydroxy-3',4'-methylenedioxyisoflavone
7-Hydroxy-3', 4'-methylenedioxyisoflavone
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H10O5/c17-10-2-3-11-14(6-10)19-7-12(16(11)18)9-1-4-13-15(5-9)21-8-20-13/h1-7,17H,8H2Key: KNJNBKINYHZUGC-UHFFFAOYSA-N
  • InChI=1/C16H10O5/c17-10-2-3-11-14(6-10)19-7-12(16(11)18)9-1-4-13-15(5-9)21-8-20-13/h1-7,17H,8H2Key: KNJNBKINYHZUGC-UHFFFAOYAK
SMILES
  • C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O
Properties
Chemical formula C16H10O5
Molar mass 282.24 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Pseudobaptigenin is an isoflavone, a type of flavonoid. It can be isolated in Trifolium pratense (red clover).

References

  1. Identification of isoflavones calycosin and pseudobaptigenin in Trifolium pratense. David R. Biggs and Geoffrey A. Lane, Phytochemistry, Volume 17, Issue 9, 1978, Pages 1683-1684
Isoflavones and their glycosides
Isoflavones
O-methylated isoflavones
Glycosides
Prenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic


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