2C-T-2

2C-T-2
Names
Preferred IUPAC name
2-[4-(Ethylsulfanyl)-2,5-dimethoxyphenyl]ethan-1-amine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.241.509 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C12H19NO2S/c1-4-16-12-8-10(14-2)9(5-6-13)7-11(12)15-3/h7-8H,4-6,13H2,1-3H3 checkY
    Key: HCWQGDLBIKOJPM-UHFFFAOYSA-N checkY
  • InChI=1/C12H19NO2S/c1-4-16-12-8-10(14-2)9(5-6-13)7-11(12)15-3/h7-8H,4-6,13H2,1-3H3
    Key: HCWQGDLBIKOJPM-UHFFFAOYAX
  • CCSc1cc(OC)c(cc1OC)CCN
Properties
C12H19NO2S
Molar mass 241.35 g/mol
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302
P264, P270, P301+P312, P330, P501
Pharmacology
Legal status
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

2C-T-2 is a psychedelic and entactogenic phenethylamine of the 2C family.[1] It was first synthesized in 1981 by Alexander Shulgin, and rated by him as one of the "magical half-dozen" most important psychedelic phenethylamine compounds.[2][3] The drug has structural and pharmacodynamic properties similar to those of 2C-T-7 ("Blue Mystic").

  1. ^ "Stolaroff's & Well's Study". erowid.org. 2001-02-06. Retrieved 2023-10-30.
  2. ^ Theobald DS, Staack RF, Puetz M, Maurer HH (September 2005). "New designer drug 2,5-dimethoxy-4-ethylthio-beta-phenethylamine (2C-T-2): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry". Journal of Mass Spectrometry. 40 (9): 1157–1172. Bibcode:2005JMSp...40.1157T. doi:10.1002/jms.890. PMID 16041763.
  3. ^ "#40 2C-T-2". Erowid Online Books : "PIHKAL".