Exploring Trichocerine. To explore a different substance…

Names:
Trichocerine
Trichocereine
N,N-Dimethylmescaline
N,N-Dimethyl-3,4,5-trimethoxyphenethylamine
IUPAC name:
N,N-Dimethyl-2-(3,4,5-trimethoxyphenyl)ethan-1-amine
263 · C13H21NO3 · 239.311
InChI=1S/C13H21NO3/c1-14(2)7-6-10-8-11(15-3)13(17-5)12(9-10)16-4/h8-9H,6-7H2,1-5H3
BTSKBPJWJZFTPQ-UHFFFAOYSA-N This stereoisomer Any stereoisomer
COc1cc(CCN(C)C)cc(c1OC)OC

Shulgin, AT. Psychotomimetic drugs: structure-activity relationships. In Handbook of Psychopharmacology: Stimulants; Iversen, LL; Iversen, SD; Snyder, SH, Eds., Plenum Press, New York, 1978; Vol. 11, pp 243–333. 2.6 MB. https://doi.org/10.1007/978-1-4757-0510-2_6 Rhodium.

Smythies, JR; Sykes, EA. Structure-activity relationship studies on mescaline: The effect of dimethoxyphenylethylamine and N,N-dimethyl mescaline on the conditioned avoidance response in the rat. Psychopharmacologia, 1 Sep 1965, 8 (5), 324-330. 371 kB. https://doi.org/10.1007/BF00453510

Shulgin, AT. Hallucinogens. In Burger’s Medicinal Chemistry, 4th ed., Part III; Wolff, ME, Ed., Wiley & Co., 1981; pp 1109–1137. 4.7 MB. #21

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

Hoffer, A; Osmond, H. The Hallucinogens, Academic Press, New York, 1967. 3.9 MB. #Trichocereine

AEM
ASB
3C-E
2C-O-4
EMM
IP
MEM
MME
MP
P
SB
189
4C-TMPEA-6
BOED
Z-7.2
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
15 October 2018 · Creative Commons BY-NC-SA ·