2C-YN

From Wikipedia, the free encyclopedia
2C-YN
2C-YN skeletal.svg
Legal status
Legal status
  • UK: Class A
Identifiers
IUPAC name
  • 2-(4-ethynyl-2,5-dimethoxyphenyl)ethanamine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC12H15NO2
Molar mass205.257 g·mol−1
3D model (JSmol)
SMILES
  • COc1cc(CCN)c(OC)cc1C#C
InChI
  • InChI=1S/C12H15NO2/c1-4-9-7-12(15-3)10(5-6-13)8-11(9)14-2/h1,7-8H,5-6,13H2,2-3H3 checkY
  • Key:MLJHHYIJBZVUEA-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  

2C-YN is an analog of phenethylamine that can be synthesized from 2C-I.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of 2C-YN, although Daniel Trachsel lists it as having a dosage of around 50mg and a duration of around 2 hours, with relatively mild psychedelic effects.[2]

Legality[]

Canada[]

As of October 31st, 2016; 2C-YN is a controlled substance (Schedule III) in Canada. http://gazette.gc.ca/rp-pr/p2/2016/2016-05-04/html/sor-dors72-eng.php

See also[]

References[]

  1. ^ Trachsel D (August 2003). "Synthesis of Novel (Phenylalkyl) amines for the Investigation of Structure–Activity Relationships, Part 3: 4‐Ethynyl‐2,5‐dimethoxyphenethylamine (= 4‐Ethynyl‐2, 5‐dimethoxybenzeneethanamine; 2C‐YN)". Helvetica Chimica Acta. 86 (8): 2754–9. doi:10.1002/hlca.200390224.
  2. ^ Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine Von der Struktur zur Funktion. Nachtschatten Verlag AG. p. 768. ISBN 978-3-03788-700-4.
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