Exploring 2C-T. To explore a different substance…

Names:
2C-T · 4-Methylthio-2,5-dimethoxyphenethylamine · 2,5-Dimethoxy-4-methylthiophenethylamine
IUPAC name:
2-[2,5-Dimethoxy-4-(methylsulfanyl)phenyl]ethan-1-amine
ID: 39 · Formula: C11H17NO2S · Molecular weight: 227.323
InChI: InChI=1S/C11H17NO2S/c1-13-9-7-11(15-3)10(14-2)6-8(9)4-5-12/h6-7H,4-5,12H2,1-3H3

Chapman, SJ; Avanes, AA. PeakAL: Protons I Have Known and Loved — Fifty Shades of Grey-Market Spectra. Supplementary Data. BLOTTER, 1 Aug 2015, 1 (1). 11.9 MB. http://dx.doi.org/10.16889/isomerdesign-1-supp Open access DOI

Chapman, SJ; Avanes, AA. PeakAL: Protons I Have Known and Loved — Fifty Shades of Grey-Market Spectra. BLOTTER, 1 Aug 2015, 1 (1). 2.6 MB. http://dx.doi.org/10.16889/isomerdesign-1 Open access DOI

Leth-Petersen, S; Bundgaard, C; Hansen, M; Carnerup, MA; Kehler, J; Kristensen, JL. Correlating the metabolic stability of psychedelic 5-HT2A agonists with anecdotal reports of human oral bioavailability. Neurochem. Res., 12 Feb 2014, 39 (10), 2018-2023. 625 kB. http://dx.doi.org/10.1007/s11064-014-1253-y

Kier, LB; Glennon, RA. Psychotomimetic phenalkylamines as serotonin agonists: An SAR analysis. Life Sci., 8 May 1978, 22 (18), 1589–1593. 238 kB. http://dx.doi.org/10.1016/0024-3205(78)90053-X

Nichols, DE; Shulgin, AT; Dyer, DC. Directional lipophilic character in a series of psychotomimetic phenethylamine derivatives. Life Sci., 1 Jan 1977, 21 (4), 569–576. 320 kB. http://dx.doi.org/10.1016/0024-3205(77)90099-6

Meyers-Riggs, B. 2C-T-X substitution size and potency. countyourculture, countyourculture: rational exploration of the underground, 1 Apr 2011.

Meyers-Riggs, B. Shulgin’s sulfur symphony—part I. countyourculture, countyourculture: rational exploration of the underground, 15 Jan 2011.

Blaazer, AR; Smid, P; Kruse, CG. Structure-activity relationships of phenylalkylamines as agonist ligands for 5-HT2A receptors. ChemMedChem, 15 Sep 2008, 3 (9), 1299–1309. 461 kB. http://dx.doi.org/10.1002/cmdc.200800133

Nichols, DE; Shulgin, AT. Sulfur analogs of psychotomimetic amines. J. Pharm. Sci., 1 Jan 1976, 65 (1), 1554–1556. 383 kB. http://dx.doi.org/10.1002/jps.2600651040 Rhodium.

25T-NBOMe
25T-NBOH
25T-NBF
25T-NBMD
ALEPH
4C-T
2CT-2ETO
2C-B
2C-C
2C-D
2C-E
2C-F
2C-H
2C-I
2C-N
2C-O-4
2C-P
2C-SE
2C-T-2
2C-T-4
2C-T-7
2C-T-8
2C-T-9
2C-T-13
2C-T-15
2C-T-17
2C-T-21
TMPEA
2C-CN
2C-CA · 2C-COOH
2C-TFM
2C-O-2
2C-O-7
2C-O-19
2C-SE-2
2C-SE-4
2C-SE-7
2C-SE-21
2C-TE
2C-T-10
2C-T-11
2C-T-12
2C-T-14
2C-T-5
2C-T-16
2C-T-6
2C-T-19
2C-T-21.5
2C-T-22
2C-T-18
2C-T-23
2C-YN
2C-pEtOH
2C-pKet
2C-T-3
2C-T-25
2C-T-27
2C-T-28
2C-T-30
2C-T-31
2C-T-32
2C-T-33
2C-VI
2C-BI-1
2C-BI-2
2C-BI-3
2C-BI-4
2C-BI-5
2C-BI-6
2C-BI-7
2C-BI-8
2C-BI-9
2C-BI-10
2C-BI-11
2C-BI-12
2326
2324
2327
2C-IP
2C-EF
2C-NH
2C-HM
2C-IB
2C-TFE
2C-O-22
2C-O-21.5
2C-O-21
2C-A
2CT-5ETO
2-TIM
3-TIM
4-TIM
3-TM
4-TM
ψ-2C-T
25T-NBOMe
25T-NBOH
25T-NBF
25T-NBMD
ALEPH
4C-T
2CT-2ETO
2C-B
2C-C
2C-D
2C-E
2C-F
2C-H
2C-I
2C-N
2C-O-4
2C-P
2C-SE
2C-T-2
2C-T-4
2C-T-7
2C-T-8
2C-T-9
2C-T-13
2C-T-15
2C-T-17
2C-T-21
TMPEA
2C-CN
2C-CA · 2C-COOH
2C-TFM
2C-O-2
2C-O-7
2C-O-19
2C-SE-2
2C-SE-4
2C-SE-7
2C-SE-21
2C-TE
2C-T-10
2C-T-11
2C-T-12
2C-T-14
2C-T-5
2C-T-16
2C-T-6
2C-T-19
2C-T-21.5
2C-T-22
2C-T-18
2C-T-23
2C-YN
2C-pEtOH
2C-pKet
2C-T-3
2C-T-25
2C-T-27
2C-T-28
2C-T-30
2C-T-31
2C-T-32
2C-T-33
2C-VI
2C-BI-1
2C-BI-2
2C-BI-3
2C-BI-4
2C-BI-5
2C-BI-6
2C-BI-7
2C-BI-8
2C-BI-9
2C-BI-10
2C-BI-11
2C-BI-12
2326
2324
2327
2C-IP
2C-EF
2C-NH
2C-HM
2C-IB
2C-TFE
2C-O-22
2C-O-21.5
2C-O-21
2C-A
2CT-5ETO
2-TIM
3-TIM
4-TIM
3-TM
4-TM
ψ-2C-T
19 November 2017 · Creative Commons BY-NC-SA ·