| 词条 | Nonahydroxytriphenic acid |
| 释义 |
| ImageFile = Nonahydroxytriphenic acid.png | ImageSize = 250px | ImageAlt = Chemical structure of nonahydroxytriphenic acid. | IUPACName = 4,4′,4′′,5,5′,5′′,6,6′,6′′-Nonahydroxy-1,1′:3′,1′′-terphenyl-2,2′,2′′-tricarboxylic acid | OtherNames = Nonahydroxytriphenoyl |Section1={{Chembox Identifiers | CASNo = | PubChem = | SMILES = 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 | ChemSpiderID = 35308523 | 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) | InChIKey = KLKCDGZVVKFBQP-UHFFFAOYAP | StdInChI = 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) | StdInChIKey = KLKCDGZVVKFBQP-UHFFFAOYSA-N |Section2={{Chembox Properties | C=21 | H=14 | O=15 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Nonahydroxytriphenic acid is a moiety found in some ellagitannins such as roburin A, B,C and D, castalagin or grandinin.[1] References1. ^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}} {{ellagitannin}}{{natural phenol-stub}} 1 : Ellagitannins |
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