Nonahydroxytriphenic acid

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Nonahydroxytriphenic acid
Chemical structure of nonahydroxytriphenic acid.
Names
IUPAC name
4,4',4,5,5',5,6,6',6-nonahydroxy-1,1':3',1-terphenyl-2,2',2-tricarboxylic acid
Other names
Nonahydroxytriphenoyl
Identifiers
ChemSpider 35308523
Jmol 3D model Interactive image
  • 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
  • InChI=1/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-UHFFFAOYAP
  • 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 506.33 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

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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