^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. doi:10.1016/0305-1978(94)90008-6.
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herniarin, natural, chemical, compound, chemically, considered, methoxy, derivative, coumarin, methyl, derivative, umbelliferone, names, preferred, iupac, name, methoxy, benzopyran, other, names, methylumbelliferone7, methoxycoumarinayapaninemethyl, umbellifer. Herniarin is a natural chemical compound Chemically it can be considered a methoxy derivative of coumarin or a methyl derivative of umbelliferone Herniarin Names Preferred IUPAC name 7 Methoxy 2H 1 benzopyran 2 one Other names 7 O Methylumbelliferone7 MethoxycoumarinAyapaninHerniarineMethyl umbelliferyl ether Identifiers CAS Number 531 59 9 Y 3D model JSmol Interactive image ChEMBL ChEMBL49732 N ChemSpider 10295 N ECHA InfoCard 100 007 741 PubChem CID 10748 UNII DGK72G008A Y 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 NKey LIIALPBMIOVAHH UHFFFAOYSA N NInChI 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 C 10H 8O 3 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 Y N Infobox references 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 edit 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 doi 10 1016 0305 1978 94 90008 6 nbsp This article about an aromatic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Herniarin amp oldid 1149385442, wikipedia, wiki, book, books, library,