6-Hydroxycyanidin
Chemical structure of 6-hydroxycyanidin
Names
IUPAC name
3,3′,4′,5,6,7-Hexahydroxyflavylium
Systematic IUPAC name
2-(3,4-Dihydroxyphenyl)-3,5,6,7-tetrahydroxy-1λ4-benzopyran-1-ylium
Other names
6-Hydroxycyanidin
Quercetagetinidin
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C15H10O7/c16-8-2-1-6(3-9(8)17)15-11(19)4-7-12(22-15)5-10(18)14(21)13(7)20/h1-5H,(H5-,16,17,18,19,20,21)/p+1 checkY
    Key: PWDAKBACEAGRSH-UHFFFAOYSA-O checkY
  • InChI=1S/C15H10O7/c16-8-2-1-6(3-9(8)17)15-11(19)4-7-12(22-15)5-10(18)14(21)13(7)20/h1-5H,(H5-,16,17,18,19,20,21)/p+1
    Key: PWDAKBACEAGRSH-IKLDFBCSAI
  • Key: PWDAKBACEAGRSH-UHFFFAOYSA-O
  • Oc1c(O)cc2[o+]c(-c(cc3O)ccc3O)c(O)cc2c1O
  • Oc1ccc(cc1O)c3[o+]c2cc(O)c(O)c(O)c2cc3O
Properties
C15H11O7
(C15H11ClO7)
Molar mass 303.24 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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6-Hydroxycyanidin is an anthocyanidin.

Glycosides

6-Hydroxycyanidin 3-malonylglucoside can be extracted from the flowers of Alstroemeria sp.[1][2]

References

  1. ^ 6-Hydroxycyanidin 3-malonylglucoside, a novel malonylanthocyanin from the flowers of Alstroemeria sp. (ca. 50 g). F. Tatsuzawa, N. Murata, K. Shinoda, N. Saito, A. Shigihara and T. Honda, Heterocycles, 2001, 55(6), pp. 1195-1199, doi:10.3987/COM-01-9225
  2. ^ Structure determination OF 6-hydroxycyanidin- and 6-hydroxydelphinidin-3-(6".O.alpha .L-rhamnopyranosyl-beta -D-glucopyranosides) and other anthocyanins from Alstroemeria cultivars. Nygatd A.-M., Aksnes D. W., Andersen O. M. and Bakken A. K., Acta chemica scandinavica, 1997, vol. 51, no. 1, pp. 108-112, INIST 10723875
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