Trifluoromescaline

Today, we want to address the topic of Trifluoromescaline, an aspect that has gained relevance in recent times and that arouses the interest of a wide spectrum of the public. From its origins to its impact on modern society, Trifluoromescaline has been the subject of debate, reflection and study. Throughout history, Trifluoromescaline has influenced various areas of life, from politics to culture, and its relevance has continued to grow. In this article, we will explore the different facets of Trifluoromescaline, examining its evolution over time and its impact today. We hope that this analysis provides a broader and enriching view on Trifluoromescaline, offering our readers a deeper understanding of this topic of universal interest.

Trifluoromescaline
Clinical data
ATC code
  • none
Identifiers
  • 2-ethanamine
PubChem CID
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC11H14F3NO3
Molar mass265.232 g·mol−1
3D model (JSmol)
  • COc1cc(CCN)cc(OC)c1OC(F)(F)F
  • InChI=1S/C11H14F3NO3/c1-16-8-5-7(3-4-15)6-9(17-2)10(8)18-11(12,13)14/h5-6H,3-4,15H2,1-2H3
  • Key:AVPVNYDXWCNFJD-UHFFFAOYSA-N

Trifluoromescaline (TF-M) is a derivative of the phenethylamine hallucinogen mescaline, which has a trifluoromethoxy group replacing the central methoxy group of mescaline. Synthesis of this compound was first reported by Daniel Trachsel in 2011, alongside many other related compounds.[1][2] Trifluoromescaline was found to be one of the most potent compounds in the series, with a reported dosage of 15–40 mg (and 60 mg being described as a "strong overdose"), and a slow onset of action and long duration of effects, lasting 14–24 hours or more.[3]

See also

References

  1. ^ Trachsel D (2002). "Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur-Aktivitätsbeziehungen, Mitteilung 1, Mescalin Derivate". Helvetica Chimica Acta. 85 (9): 3019–3026. doi:10.1002/1522-2675(200209)85:9<3019::AID-HLCA3019>3.0.CO;2-4.
  2. ^ Trachsel D (2012). "Fluorine in psychedelic phenethylamines". Drug Testing and Analysis. 4 (7–8): 577–590. doi:10.1002/dta.413. PMID 22374819.
  3. ^ Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 704–723. ISBN 978-3-03788-700-4.