Names:
4-TASB
4-Thioasymbescaline
3-Ethoxy-4-ethylthio-5-methoxyphenethylamine
IUPAC name:
2-[3-Ethoxy-4-(ethylsulfanyl)-5-methoxyphenyl]ethan-1-amine
147 · C13H21NO2S · 255.376
InChI=1S/C13H21NO2S/c1-4-16-12-9-10(6-7-14)8-11(15-3)13(12)17-5-2/h8-9H,4-7,14H2,1-3H3
IUZSEPUWBBUJME-UHFFFAOYSA-N This stereoisomer Any stereoisomer
NCCc1cc(OCC)c(c(c1)OC)SCC

Jacob, P; Shulgin, AT. Sulfur analogues of psychotomimetic agents. 3. Ethyl homologues of mescaline and their monothioanalogues. J. Med. Chem., 1 Jan 1984, 27 (7), 881–887. 1.2 MB. https://doi.org/10.1021/jm00373a013

Thakur, M; Thakur, A; Khadikar, PV. QSAR studies on psychotomimetic phenylalkylamines. Bioorg. Med. Chem., 15 Feb 2004, 12 (4), 825–831. 323 kB. https://doi.org/10.1016/j.bmc.2003.10.027

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.

Jacob, P; Shulgin, AT. Structure-activity relationships of the classic hallucinogens and their analogs. In Hallucinogens: An update. NIDA Research Monograph 146; Lin, GC; Glennon, RA, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 1994; pp 74–91. 51 kB.

ALEPH-2
2C-T-4
ψ-2C-T-4
2C-T-7
3-TASB
5-TASB
TP
3-TSB
4-TSB
2CT2-2ETO
2CT2-5ETO
4C-T
2,4,3-2C-T-7
3,4,2-2C-T-7
2,3,4-2C-T-7
3,5,2-2C-T-7
2,3,5-2C-T-7
4,5,2-2C-T-7
N-Me-ALEPH
3,4,5-2C-T-7
2,6,3-2C-T-7
3,6,2-2C-T-7
2,3,6-2C-T-7
4,6,2-2C-T-7
ψ-ALEPH-2
ψ-2C-T-7
DOMeSM
3-TIP
p4-646: 4-TASB
12 November 2018 · Creative Commons BY-NC-SA ·