Anodyne

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2C-T-2
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
241.35 g/mol [1]
2.1 [1]
Structural Identifiers
[]
C12H19NO2S [1]
2-(4-ethylsulfanyl-2,5-dimethoxyphenyl)ethanamine [1]
CCSC1=C(C=C(C(=C1)OC)CCN)OC [1]
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 [1]
InChIKeyHCWQGDLBIKOJPM-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-ethylthiophenethylamine

2,5-Dimethoxy-4-ethylthiophenethylamine (also known as 811-235-0, 2,5-Dimethoxy-4-(ethylthio)phenethylamine, 2C-T-2, 2,5-Dimetoxy-4-ethylthiophenethlamine, 2C-T2, Benzeneethanamine, 4-(ethylthio)-2,5-dimethoxy-, Rosy, 2,5-Dimethoxy-4-ethylthiophenylamine, J1.114.642b or 2-(4-(ethylthio)-2,5-dimethoxyphenyl)ethan-1-amine) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

Salts []

2,5-Dimethoxy-4-ethylthiophenethylamine is typically found in the form of its hydrochloride salt.

 []

2,5-Dimethoxy-4-ethylthiophenethylamine is a achiral mixture

See also []

  • 4-Substituted 2,5-dimethoxyphenethylamines (2C-x)
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 12074193, 2,5-Dimethoxy-4-ethylthiophenethylamine. Accessed July 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/12074193

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-ethylthiophenethylamine. UNII: WPS2KSX2TJ. Global Substance Registration System. Accessed July 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/WPS2KSX2TJ