Hypolaetin

Hypolaetin
	Chemical structure of hypolaetin.
Names
	IUPAC name 2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxychromen-4-one
	Other names 8-Hydroxyluteolin
Identifiers
CAS Number	27696-41-9
ChemSpider	4444967
Jmol 3D model	Interactive image
PubChem	5281648
	InChI InChI=1S/C15H10O7/c16-7-2-1-6(3-8(7)17)12-5-10(19)13-9(18)4-11(20)14(21)15(13)22-12/h1-5,16-18,20-21H Key: ASOIXDIITRKTOX-UHFFFAOYSA-N ; InChI=1/C15H10O7/c16-7-2-1-6(3-8(7)17)12-5-10(19)13-9(18)4-11(20)14(21)15(13)22-12/h1-5,16-18,20-21H Key: ASOIXDIITRKTOX-UHFFFAOYAN ;
	SMILES C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O ;
Properties
Chemical formula	C15H10O7
Molar mass	302.23 g/mol
Vapor pressure	{{{value}}}
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Hypolaetin is a flavone. It is the aglycone of hypolaetin 8-glucuronide, a compound found in the liverwort Marchantia berteroana.^[1] Hypolaetin 8-glucoside can be found in Sideritis leucantha.^[2]

References

Cite error: Invalid <references> tag; parameter "group" is allowed only.

Use <references />, or <references group="..." />

This article about a phenol is a stub. You can help Wikipedia by expanding it.

↑ Isoscutellarein and hypolaetin 8-glucuronides from the liverwort Marchantia berteroana. Kenneth R. Markham and Lawrence J. Porter, Phytochemistry, April 1975, Volume 14, Issue 4, Pages 1093–1097, doi:10.1016/0031-9422(75)85194-6
↑ Hypolaetin 8-glucoside from Sideritis leucantha. Francisco Tomas, Bernard Voirina, Francisco A.T. Barberan and Philippe Lebreton, Phytochemistry, 1985, Volume 24, Issue 7, Pages 1617–1618, doi:10.1016/S0031-9422(00)81082-1