Exploring 5,6-MDO-DMT. To explore a different substance…

Names:
5,6-MDO-DMT
Tryptamine, N,N-dimethyl-5,6-methylenedioxy
Indole, 3-[2-(dimethylamino)ethyl]-5,6-methylenedioxy
N,N-Dimethyl-5,6-methylenedioxytryptamine
3-[2-(Dimethylamino)ethyl]-5,6-methylenedioxyindole
5H-1,3-Dioxolo-[4,5-f]indole-7-ethanamine, N,N-dimethyl
IUPAC names:
2-(2H,5H-[1,3]Dioxolo[4,5-f]indol-7-yl)-N,N-dimethylethan-1-amine
2-(5H-[1,3]Dioxolo[4,5-f]indol-7-yl)-N,N-dimethylethan-1-amine
ID: 5031 · Formula: C13H16N2O2 · Molecular weight: 232.278
InChI: InChI=1S/C13H16N2O2/c1-15(2)4-3-9-7-14-11-6-13-12(5-10(9)11)16-8-17-13/h5-7,14H,3-4,8H2,1-2H3
InChI Key: QHEIGHVZMWJQHB-UHFFFAOYSA-NThis stereoisomerAny stereoisomer

Kline, TB; Benington, F; Morin, RD; Beaton, JM; Glennon, RA; Domelsmith, LN; Houk, KN; Rozeboom, MD. Structure-activity relationships for hallucinogenic N,N-dialkyltryptamines: photoelectron spectra and serotonin receptor affinities of methylthio and methylenedioxy derivatives. J. Med. Chem., 1 Jan 1982, 25 (11), 1381–1383. 378 kB. https://doi.org/10.1021/jm00353a021

Kline, TB; Benington, F; Morin, RD; Beaton, JM. Structure-activity relationships in potentially hallucinogenic N,N-dialkyltryptamines substituted in the benzene moiety. J. Med. Chem., 1 Jan 1982, 25 (8), 908–913. 845 kB. https://doi.org/10.1021/jm00350a005

Grotjahn, DB. Synthesis and characterization of 5H-1,3-dioxolo[4,5-f]indoleethylamines. J. Heterocycl. Chem., 1 Jul 1982, 20 (4), 1031–1036. 517 kB. https://doi.org/10.1002/jhet.5570200438

4,5-MDO-DMT
Melatonin
5-Formylpsilocin
7-Formylpsilocin
5750
5899
MDMCM
27 May 2018 · Creative Commons BY-NC-SA ·