Herniarin

Herniarin
	Chemical structure of herniarin
Names
	Preferred IUPAC name 7-Methoxy-2H-1-benzopyran-2-one
	Other names 7-O-Methylumbelliferone; 7-Methoxycoumarin; Ayapanin; Herniarine; Methyl umbelliferyl ether
Identifiers
CAS Number	531-59-9 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL49732 ;
ChemSpider	10295 ;
ECHA InfoCard	100.007.741
PubChem CID	10748;
UNII	DGK72G008A ;
CompTox Dashboard (EPA)	DTXSID5060196 ;
	InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 Key: LIIALPBMIOVAHH-UHFFFAOYSA-N ; InChI=1/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 Key: LIIALPBMIOVAHH-UHFFFAOYAW;
	SMILES O=C/2Oc1cc(OC)ccc1\C=C\2;
Properties
Chemical formula	C10H8O3
Molar mass	176.171 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Herniarin is a natural chemical compound. Chemically, it can be considered a methoxy derivative of coumarin or a methyl derivative of umbelliferone.

Herniarin is found in Herniaria glabra,^[1] Ayapana triplinervis and in species of the genus Prunus (P. mahaleb, P. pensylvanica, and P. maximowiczii).^[2]

References

↑ "Herniarin". liberherbarum.com.
↑ Santamour F. S. and Riedel L. G. H. (1994). "Distribution and inheritance of scopolin and herniarin in some Prunus species". Biochemical Systematics and Ecology. 22 (2): 197–201. Bibcode:1994BioSE..22..197S. doi:10.1016/0305-1978(94)90008-6.

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