Exploring AEM. To explore a different substance…

Names:
AEM
α-Ethylmescaline
1-(3,4,5-Trimethoxyphenyl)-2-aminobutane
α-Ethyl-3,4,5-trimethoxyphenethylamine
2-Amino-1-(3,4,5-trimethoxyphenyl)butane
IUPAC name:
1-(3,4,5-Trimethoxyphenyl)butan-2-amine
1 · C13H21NO3 · 239.311
InChI=1S/C13H21NO3/c1-5-10(14)6-9-7-11(15-2)13(17-4)12(8-9)16-3/h7-8,10H,5-6,14H2,1-4H3
DCYONQVUAUEKAJ-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Shulgin, AT. Psychotomimetic agents related to mescaline. Experientia, 1 Jan 1963, 19 (3), 127–128. 264 kB. https://doi.org/10.1007/BF02171586

Shulgin, AT; Sargent, T; Naranjo, C. Structure-activity relationships of one-ring psychotomimetics. Nature, 1 Jan 1969, 221, 537–541. 537 kB. https://doi.org/10.1038/221537a0

Daley, PF; Morris, H. Pages from the lab notebook of Alexander Shulgin: A glance through the history of psychedelic chemistry. Vice, 1 Oct 2012.

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.

Nichols, DE. Medicinal chemistry and structure-activity relationships. In Amphetamine and its Analogs; Cho, AK; Segal, DS, Eds., Academic Press, San Diego, CA, 1994; pp 3–41. 6.9 MB.

Shulgin, AT. Psychotomimetic agents. In Psychopharmacological Agents; Gordon, M, Ed., Academic Press, New York, 1976; Vol. 4, pp 59–146. 3.1 MB. #LXII

ASB
3C-E
2C-O-4
EMM
IP
MEM
MME
MP
P
SB
189
4C-TMPEA-6
BOED
Z-7.2
Trichocerine
N-Me-TMA · METHYL-TMA
N-Me-TMA-2 · METHYL-TMA-2
N-Me-TMA-6 · METHYL-TMA-6
2C-O-7
Salbutamol
homo-TMA-2
homo-TMA-3
homo-TMA-6
N,N-Me-β,3,4-TMPEA
β-HO-β,N,N-Me-2,5-DMPEA
β-HO-N,N-Me-2,5-DMA
β-HO-N-Me-2,5-DEPEA
β-HO-2,5-DEA
N-Me-TMA-3
4C-TMPEA-3
4C-HM
BOE
DOEH
4C-TMA-2
DESMETHYL-iPr
α-MM-M
ψ-MEM
DOMOM
10453
DMe-M
10404
MIP · Metaisoproscaline
β,β-Dimethylmescaline
2C-EOM
19 August 2018 · Creative Commons BY-NC-SA ·