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Names

(C4) RCS-4
RCS-4-C4
4MeO-PH-BIMO

IUPAC name

(1-Butyl-1H-indol-3-yl)(4-methoxyphenyl)methanone

ID 4702 · Formula C₂₀H₂₁NO₂ · Molecular weight 307.386

Tags Cannabinoid

InChI InChI=1S/C20H21NO2/c1-3-4-13-21-14-18(17-7-5-6-8-19(17)21)20(22)15-9-11-16(23-2)12-10-15/h5-12,14H,3-4,13H2,1-2H3

InChI Key INTUAOVLJFCJIP-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CCCCn1cc(c2c1cccc2)C(=O)c1ccc(cc1)OC

ChemSpider 29341521
PubChem 57507905
Project Response RCS-4 (C4) (1231-15)
Project Response RCS-4 (C4-homolog) (1957-18)

EMCDDA. New drugs in Europe, 2011, European Monitoring Centre for Drugs and Drug Addiction, Lisbon, 1 Apr 2012. 401 kB.

Banister, SD; Connor, M. The chemistry and pharmacology of synthetic cannabinoid receptor agonists as new psychoactive substances: Origins In New Psychoactive Substances: Pharmacology, Clinical, Forensic and Analytical Toxicology; Maurer, HH; Brandt, SD, Eds., Springer, Berlin, Heidelberg, 1 Jan 2018; pp 165-190. 906 kB. https://doi.org/10.1007/164_2018_143 #61

Abbate, V; Schwenk, M; Presley, BC; Uchiyama, N. The ongoing challenge of novel psychoactive drugs of abuse. Part I. Synthetic cannabinoids (IUPAC Technical Report) Pure Appl. Chem., 28 Aug 2018, 90 (8), 1255–1282. 1.0 MB. https://doi.org/10.1515/pac-2017-0605 #3. RCS-4 butyl homolog

Banister, SD; Stuart, J; Conroy, T; Longworth, M; Manohar, M; Beinat, C; Wilkinson, SM; Kevin, RC; Hibbs, DE; Glass, M; Connor, M; McGregor, IS; Kassiou, M. Structure–activity relationships of synthetic cannabinoid designer drug RCS-4 and its regioisomers and C4 homologues Forensic Toxicol., 1 Jul 2015, 33 (2), 355–366. 931 kB. https://doi.org/10.1007/s11419-015-0282-9 #RCS-4-C4 GC,MS,NMR,IR,UV,other

2,5-Dimethoxy-4-(naphthalen-2-yl)phenethylamine · 2C-BI-5

(C4) ortho-RCS-4 · RCS-2-C4

RCS-3-C4

7 Dec 2019 · · Isomer Design