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Herniarin

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(Redirected from 7-Methoxycoumarin)
Herniarin
Chemical structure of 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
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.007.741 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3Key: LIIALPBMIOVAHH-UHFFFAOYSA-N
  • InChI=1/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3Key: LIIALPBMIOVAHH-UHFFFAOYAW
SMILES
  • O=C/2Oc1cc(OC)ccc1\C=C\2
Properties
Chemical formula C10H8O3
Molar mass 176.171 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

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, Ayapana triplinervis and in species of the genus Prunus (P. mahaleb, P. pensylvanica, and P. maximowiczii).

References

  1. "Herniarin". liberherbarum.com.
  2. 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.
Types of coumarins
Aglycones
O-Methylated
Glycosides
Derivatives
Furanocoumarins
Aglycones
O-Methylated
Furanocoumarin glycosides
Meroterpene furanocoumarin ether
Oligomers
Synthetic


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