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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
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).
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