Nonahydroxytriphenic acid
Chemical structure of nonahydroxytriphenic acid.
Names
Preferred IUPAC name
14,15,16,23,24,25,34,35,36-Nonahydroxy[11,21:23,31-terphenyl]-12,22,32-tricarboxylic acid
Other names
Nonahydroxytriphenoyl
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C21H14O15/c22-5-1-3(19(31)32)7(14(26)12(5)24)9-11(21(35)36)10(17(29)18(30)16(9)28)8-4(20(33)34)2-6(23)13(25)15(8)27/h1-2,22-30H,(H,31,32)(H,33,34)(H,35,36)
    Key: KLKCDGZVVKFBQP-UHFFFAOYSA-N
  • Oc2c(c1c(cc(O)c(O)c1O)C(=O)O)c(c(c(O)c2O)c3c(cc(O)c(O)c3O)C(=O)O)C(=O)O
Properties
C21H14O15
Molar mass 506.328 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Nonahydroxytriphenic acid is a moiety found in some ellagitannins such as roburin A, B,C and D, castalagin or grandinin.[1]

References

  1. ^ Roburin A, a dimeric ellagitannin from heartwood of Quercus robur. Hervé Du Penhoat, Michon V. M. F., Ohassan A., Shuyun Peng, Scalbert A. and Gage D., Phytochemistry, 1991, vol. 30, no 1, pages 329-332, INIST 19775624


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