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).
Infobox references
Nonahydroxytriphenic acid is a moiety found in some ellagitannins such as roburin A , B,C and D, castalagin or grandinin .[ 1]
References ^ 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 FPedunculagin Punicalagin Punigluconin Phyllanemblinin A, B, C, D, E and F Punicalin Roburin E Rugosin E Sanguiin H-5 Stenophyllanin A , B and CStrictinin Tellimagrandin I and II Teracatain Terchebulin Terflavin A and B Tergallic acid Tergallic acid dilactone C-glycosidic ellagitannins Dehydroellagitannins (molecules withdehydrohexahydroxydiphenic acid (DHHDP) Transformed ellagitannins
molecules with chebulic acid molecules with Elaeocarpusinic acid Elaeocarpusin Helioscopin B Mallojaponin (1-O-Galloyl-2,4-elaeocarpusinoyl-3,6-(R)-valoneayl-beta-D-glucose)
Oligomers Other
