2C-T-3

In today's world, 2C-T-3 has become a topic of growing interest in different areas of society. From the academic environment to the business environment, 2C-T-3 is becoming relevant due to its impact on our daily lives. As we continue to move forward into the 21st century, the importance of understanding and addressing 2C-T-3 becomes increasingly evident. In this article, we will explore how 2C-T-3 has evolved over time, its impact on different communities and sectors, and possible implications for the future. From its influence on politics to its impact on technology, 2C-T-3 is a topic that deserves our attention and reflection.

2C-T-3
Names
Preferred IUPAC name
2-{2,5-Dimethoxy-4-phenyl}ethan-1-amine
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C14H21NO2S/c1-10(2)9-18-14-8-12(16-3)11(5-6-15)7-13(14)17-4/h7-8H,1,5-6,9,15H2,2-4H3
    Key: JCDUUDQZKIXJJP-UHFFFAOYSA-N
  • CC(=C)CSC1=C(C=C(C(=C1)OC)CCN)OC
Properties
C14H21NO2S
Molar mass 267.39 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

2C-T-3, also initially numbered as 2C-T-20 and also known as 4-methallylthio-2,5-dimethoxyphenethylamine, is a lesser-known psychedelic drug related to compounds such as 2C-T-7 and 2C-T-16. It was named by Alexander Shulgin but was never made or tested by him, and was instead first synthesised by Daniel Trachsel some years later. It has a binding affinity of 11nM at 5-HT2A and 40nM at 5-HT2C. It is reportedly a potent psychedelic drug with an active dose in the 15–40 mg range, and a duration of action of 8–14 hours, with visual effects comparable to related drugs such as methallylescaline.[1][2][3]

See also

References

  1. ^ Trachsel D (2003). "Synthesis of novel (phenylalkyl)amines for the investigation of structure-activity relationships. Part 2. 4-Thio-substituted amines (=2,5-dimethoxybenzeneethanamines)". Helvetica Chimica Acta. 86 (7): 2610–2619. doi:10.1002/hlca.200390210.
  2. ^ Luethi D, Trachsel D, Hoener MC, Liechti ME (May 2018). "Monoamine receptor interaction profiles of 4-thio-substituted phenethylamines (2C-T drugs)" (PDF). Neuropharmacology. 134 (Pt A): 141–148. doi:10.1016/j.neuropharm.2017.07.012. PMID 28720478. S2CID 7135811.
  3. ^ Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine: Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 788–794. ISBN 978-3-03788-700-4.


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