Exploring META-DOT. To explore a different substance…

Names:
m-DOT
META-DOT
2,4-Dimethoxy-5-methylthioamphetamine
5-Methylthio-2,4-dimethoxyamphetamine
IUPAC name:
1-[2,4-Dimethoxy-5-(methylsulfanyl)phenyl]propan-2-amine
125 · C12H19NO2S · 241.35
InChI=1S/C12H19NO2S/c1-8(13)5-9-6-12(16-4)11(15-3)7-10(9)14-2/h6-8H,5,13H2,1-4H3
BEMIKIUJWHLJTP-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Jacob, P; Anderson, G; Meshul, CK; Shulgin, AT; Castagnoli, N. Monomethylthio analogues of 1-(2,4,5-trimethoxyphenyl)-2-aminopropane. J. Med. Chem., 1 Jan 1977, 20 (10), 1235–1239. 717 kB. https://doi.org/10.1021/jm00220a001

Domelsmith, LN; Eaton, TA; Houk, KN; Anderson, GM; Glennon, RA; Shulgin, AT; Castagnoli, N; Kollman, PA. Photoelectron spectra of psychotropic drugs. 6. Relationships between physical properties and pharmacological actions of amphetamine analogues. J. Med. Chem., 1 Jan 1981, 24 (12), 1414–1421. 963 kB. https://doi.org/10.1021/jm00144a009

Shulgin, AT. Basic Pharmacology and Effects. In Hallucinogens. A Forensic Drug Handbook; Laing, R; Siegel, JA, Eds., Academic Press, London, 2003; pp 67–137. 6.3 MB.

Anderson, GM; Castagnoli, N; Kollman, PA. Quantitative structure-activity relationships in the 2,4,5-ring-substituted phenylisopropylamines. In QuaSAR: Quantitative Structure Activity Relationships of Analgesics, Narcotic Antagonists, and Hallucinogens. NIDA Research Monograph 22; Barnett, G; Trsic, M; Willette, RE, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 1978; pp 199–217. 623 kB. #7

ALEPH
2C-T-2
o-DOT · ORTHO-DOT
3-TE
4-TE
3-TME
4-TME
5-TME
5-TOMSO · TOMSO
2CT-2ETO
2CT-5ETO
ψ-ALEPH
DOHSM
α-Methyl-4-TM
3,4-Dimethoxy-5-methylthioamphetamine; 3-T-TMA
24 September 2018 · Creative Commons BY-NC-SA ·