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 
 
 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).
 
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 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  
 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