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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
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
C 21 H 14 O 15
Molar mass
−1
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Nonahydroxytriphenic acid is a moiety found in some ellagitannins such as roburin A , B,C and D, castalagin or grandinin .[ 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
Moieties Lactones Monomers
Acetonyl geraniin Alnusiin Bicornin Carlesiin Casuarictin Emblicanin A and B Euscaphinin Galloyl pedunculagin Grandinin Helioscopinin B Jolkinin Lagerstannin A , B and C Macranganin Myrobalanitannin Nupharin A , B , C , D , E and F Pedunculagin Punicalagin Punigluconin Phyllanemblinin A , B , C , D , E and F Punicalin Roburin E Rugosin E Sanguiin H-5 Stenophyllanin A , B and C Strictinin Tellimagrandin I and II Teracatain Terchebulin Terflavin A and B Tergallic acid Tergallic acid dilactone
Oligomers Other
