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Trifucol

From Wikipedia, the free encyclopedia
Trifucol
Chemical structure of trifucol
Names
Preferred IUPAC name
[11,21:23,31-Terphenyl]-12,14,16,22,24,26,32,34,36-nonol
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C18H14O9/c19-6-1-8(21)14(9(22)2-6)16-12(25)5-13(26)17(18(16)27)15-10(23)3-7(20)4-11(15)24/h1-5,19-27H
    Key: COTZPIUJHGYKAQ-UHFFFAOYSA-N
  • C1=C(C(=C(C(=C1O)C2=C(C=C(C=C2O)O)O)O)C3=C(C=C(C=C3O)O)O)O
Properties
C18H14O9
Molar mass374.29 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Trifucol is aphlorotannin found in the brown algaeScytothamnus australis andAnalipus japonicus.[1][2]


References

[edit]
  1. ^Glombitza, Karl-Werner; Rösener, Hans-Udo; Koch, Marieluise (1976). "Polyhydroxyoligophenyle und phenyläther ausBifurcaria bifurcata".Phytochemistry (in German).15 (8):1279–1281.Bibcode:1976PChem..15.1279G.doi:10.1016/0031-9422(76)85094-7.
  2. ^Pal Singh, Inder; Bharate, Sandip B. (2006). "Phloroglucinol compounds of natural origin".Natural Product Reports.23 (4):558–591.doi:10.1039/B600518G.PMID 16874390.
Types ofphlorotannins (tannins in brown algae)
Monomer
Fucols
Phlorethols
Fucophlorethols
Fuhalols
Isofuhalols
Eckols
Halogenated phlorotannins
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