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Names

25T4-NBOMe
N-(2-Methoxybenzyl)-4-isopropylthio-2,5-dimethoxyphenethylamine
2C-T-4-NBOMe

IUPAC names

2-{2,5-Dimethoxy-4-[(propan-2-yl)sulfanyl]phenyl}-N-[(2-methoxyphenyl)methyl]ethan-1-amine
2-[2,5-Dimethoxy-4-(propan-2-ylsulfanyl)phenyl]-N-(2-methoxybenzyl)ethan-1-amine

ID 5544 · Formula C₂₁H₂₉NO₃S · Molecular weight 375.525

InChI InChI=1S/C21H29NO3S/c1-15(2)26-21-13-19(24-4)16(12-20(21)25-5)10-11-22-14-17-8-6-7-9-18(17)23-3/h6-9,12-13,15,22H,10-11,14H2,1-5H3

InChI Key BOWHVFJVXBVJCU-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES COc1cc(SC(C)C)c(cc1CCNCc1ccccc1OC)OC

PubChem 125181243
Wikipedia, see 25-NB
Project Response 2C-T-4-NBOMe (1335-16)
bluelight.org The Small & Handy 25T4-NBOMe Thread

Anon. JW, Personal communication of unpublished research 1 Dec 2011.

Casale, JF; Hays, PA. Characterization of eleven 2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (NBOMe) derivatives and differentiation from their 3- and 4-methoxybenzyl analogues—Part I Microgram J., 1 Jan 2012, 9 (2), 84–109. 4.6 MB. #28: 25T4-NB2OMe GC,MS,IR

Hays, PA; Casale, JF. Characterization of eleven 2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (NBOMe) derivatives and differentiation from their 3-and 4-methoxybenzyl analogues - Part II Microgram J., 1 Jan 2014, 11 (1–4), 3–22. 8.1 MB. #28: 25T4-NB2OMe NMR

Rickli, A; Luethi, D; Reinisch, J; Buchy, D; Hoener, MC; Liechti, ME. Receptor interaction profiles of novel N-2-methoxybenzyl (NBOMe) derivatives of 2,5-dimethoxy-substituted phenethylamines (2C drugs) Neuropharmacology, 1 Dec 2015, 99, 546–553. 625 kB. https://doi.org/10.1016/j.neuropharm.2015.08.034 #25T4-NBOMe

Adamowicz, P; Zuba, D. Discrimination among designer drug isomers by chromatographic and spectrometric methods In Chromatographic Techniques in the Forensic Analysis of Designer Drugs; Kowalska, T; Sajewicz, M; Sherma, J, Eds., CRC Press, Taylor & Francis Group, 1 Jan 2018; pp 211–232. 1.1 MB. LC,MS,IR,UV

Grumann, C; Auwärter, V. Separation of positional isomers of nine 2-phenethylamine-derived designer drugs by liquid chromatography-tandem mass spectrometry Drug Test. Anal., 1 Jul 2018, 10 (7), 1184–1191. 861 kB. https://doi.org/10.1002/dta.2371 #25T4-NBOMe LC,MS

Luethi, D; Liechti, ME. Monoamine transporter and receptor interaction profiles in vitro predict reported human doses of novel psychoactive stimulants and psychedelics Int. J. Neuropsychoph., 1 Oct 2018, 21 (10), 926–931. 254 kB. https://doi.org/10.1093/ijnp/pyy047 #S2 Phenethylamines 25T4-NBOMe

Åstrand, A; Guerrieri, D; Vikingsson, S; Kronstrand, R; Green, H. In vitro characterization of new psychoactive substances at the μ-opioid, CB1, 5HT_1A, and 5-HT2_A receptors—On-target receptor potency and efficacy, and off-target effects Forensic Sci. Int., 1 Dec 2020, 317, 110553. 1.7 MB. https://doi.org/10.1016/j.forsciint.2020.110553 #25T4-NBOMe

25T7-NBOMe · 2C-T-7-NBOMe · N-(2-Methoxybenzyl)-4-propylthio-2,5-dimethoxyphenethylamine

25T4-NB3OMe · N-(3-Methoxybenzyl)-4-isopropylthio-2,5-dimethoxyphenethylamine

25T4-NB4OMe · N-(4-Methoxybenzyl)-4-isopropylthio-2,5-dimethoxyphenethylamine

25T7-NB3OMe · N-(3-Methoxybenzyl)-4-propylthio-2,5-dimethoxyphenethylamine

25T7-NB4OMe · N-(4-Methoxybenzyl)-4-propylthio-2,5-dimethoxyphenethylamine

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7 Dec 2019 · · Isomer Design