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Herniarin
Names
👁 Chemical structure of herniarin Chemical structure of herniarin
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^{👁 check Y}
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL49732^{👁 ☒ N}
ChemSpider	10295^{👁 ☒ N}
ECHA InfoCard	100.007.741 👁 Edit this at Wikidata
PubChem CID	10748
UNII	DGK72G008A^{👁 check Y}
CompTox Dashboard (EPA)	DTXSID5060196 👁 Edit this at Wikidata
InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3^{👁 ☒ N} Key: LIIALPBMIOVAHH-UHFFFAOYSA-N^{👁 ☒ 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). 👁 ☒ N verify (what is ^{👁 check Y👁 ☒ N} ?) 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.