Trifucol

The topic of Trifucol is one that has been studied, debated and analyzed for years. The importance of Trifucol is reflected in various aspects of society, from politics to popular culture. As interest in Trifucol continues to grow, it is crucial to understand its impact on our lives. In this article, we will explore different facets of Trifucol and its relevance in the modern world. From its history to its future implications, we will examine in detail how Trifucol has shaped and continues to shape our environment.

Trifucol
Chemical structure of trifucol
Names
Preferred IUPAC name
-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 mass 374.29 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Trifucol is a phlorotannin found in the brown algae Scytothamnus australis and Analipus japonicus.[1][2]


References

  1. ^ Glombitza, Karl-Werner; Rösener, Hans-Udo; Koch, Marieluise (1976). "Polyhydroxyoligophenyle und phenyläther aus Bifurcaria 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.
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