Capensinidin: Difference between revisions

Capensinidin
Names
	IUPAC name 3,4′,7-Trihydroxy-3′,5,5′-trimethoxyflavylium
	Systematic IUPAC name 3,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-1λ4-benzopyran-1-ylium
	Other names Capensinidin chloride
Identifiers
CAS Number	19077-85-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:3367 ;
ChemSpider	390280 ;
KEGG	C08595 ;
PubChem CID	441658;
CompTox Dashboard (EPA)	DTXSID00331604 ;
	InChI InChI=1S/C18H16O7/c1-22-13-6-10(19)7-14-11(13)8-12(20)18(25-14)9-4-15(23-2)17(21)16(5-9)24-3/h4-8H,1-3H3,(H2-,19,20,21)/p+1 Key: GYLVPQXQQPMCKK-UHFFFAOYSA-O ; InChI=1/C18H16O7/c1-22-13-6-10(19)7-14-11(13)8-12(20)18(25-14)9-4-15(23-2)17(21)16(5-9)24-3/h4-8H,1-3H3,(H2-,19,20,21)/p+1 Key: GYLVPQXQQPMCKK-IKLDFBCSAS;
	SMILES Oc1cc2c(OC)cc(O)cc2[o+]c1c3cc(OC)c(O)c(OC)c3;
Properties
Chemical formula	C18H17O7+ (Cl−)
Molar mass	345.32 g/mol
	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

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Latest revision as of 01:16, 30 April 2023

Capensinidin (Cp) is an O-methylated anthocyanidin. It is a water-soluble, blue-red plant dye. It is a 5-methoxy analog of malvidin, has been obtained from Plumbago capensis.^[1]

^ "Two new naturally occurring anthocyanidins". Chemical Industry: 229–230. 1960.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

@@ Line 7: / Line 7: @@
 | ImageSize = 250px
 | IUPACName = 3,4′,7-Trihydroxy-3′,5,5′-trimethoxyflavylium
-| PIN = 3,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-1λ<sup>4</sup>-benzopyran-1-ylium
+| SystematicName = 3,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-1λ<sup>4</sup>-benzopyran-1-ylium
 | OtherNames = Capensinidin chloride
 |Section1={{Chembox Identifiers
@@ Line 52: / Line 52: @@
 {{anthocyanins}}
-[[Category:O-Methylated anthocyanidins]]
+[[Category:O-methylated anthocyanidins]]