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

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. http://dx.doi.org/10.1002/jhet.5570200438

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. http://dx.doi.org/10.1021/jm00350a005

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. http://dx.doi.org/10.1021/jm00353a021

5,6-MDO-DIPT
5,6-MDO-MIPT
5,6-MDO-NC3T
5,6-MDO-MC3T
5,6-MDO-MC4T
5,6-MDO-MC3MT
5,6-MDO-MC5T
5,6-MDO-MBZT
5,6-MDO-C3BZT
5,6-MeO-DMT
5213
5,6-MDO-pyr-T
5,6-MDO-pip-T
5,6-MDO-mor-T
5,6-MDO-phpipaz-T
5,6-MDO-bzpipiz-T
5276
4,5-MDO-DMT
Melatonin
5-Formylpsilocin
7-Formylpsilocin
5750
5899
5,6-MDO-DIPT
5,6-MDO-MIPT
5,6-MDO-NC3T
5,6-MDO-MC3T
5,6-MDO-MC4T
5,6-MDO-MC3MT
5,6-MDO-MC5T
5,6-MDO-MBZT
5,6-MDO-C3BZT
5,6-MeO-DMT
5213
5,6-MDO-pyr-T
5,6-MDO-pip-T
5,6-MDO-mor-T
5,6-MDO-phpipaz-T
5,6-MDO-bzpipiz-T
5276
4,5-MDO-DMT
Melatonin
5-Formylpsilocin
7-Formylpsilocin
5750
5899
20 September 2017 · Creative Commons BY-NC-SA ·