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«Cannabicyclohexanol»
CSA Names: Cannabicyclohexanol
CP 47,497 C8 homologue
5-(1,1-Dimethyloctyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol
5-(1,1-Dimethyloctyl)-2-(3-hydroxycyclohexyl)-phenol
CSA Location: Schedule I Section (g) Subsection (2) DEA code 7298
CSA History: S. 3187, 112 Cong., 2nd Sess. added effective 9 Jul 2012
78 FR 664 finalized the prior interim scheduling effective 4 Jan 2013
Names: CP 47,497 (dimethyloctyl homologue) (primary)
2-[(1S,3R)-3-Hydroxycyclohexyl]-5-(2-methylnonan-2-yl)phenol (IUPAC)
Molecular formula: C22H36O2
Nominal mass: 332
Average mass: 332.5200
Monoisotopic mass: 332.271530
CAS registry number: 70434-92-3
ChemSpider:
PubChem: 23986041
Wikipedia: Cannabicyclohexanol
Erowid: Spice Product
Drugs-Forum:
Bluelight:
Standard InChI: InChI=1S/C22H36O2/c1-4-5-6-7-8-14-22(2,3)18-12-13-20(21(24)16-18)17-10-9-11-19(23)15-17/h12-13,16-17,19,23-24H,4-11,14-15H2,1-3H3/t17-,19+/m0/s1
Standard InChI key: HNMJDLVMIUDJNH-PKOBYXMFSA-N
SMILES: CCCCCCCC(c1ccc(c(c1)O)[C@H]1CCC[C@H](C1)O)(C)C
Tags: USCSA,cannabinoid,S.3187
 
Property Value Remarks
Property Value Remarks
Location Type Remarks
CP 47,497 (n=8 homolog) ATR IR.pdf ATR IR Thermo Nicolet
CP47497DMOH.pdf EI MS Agilent MSD
13216-0425163-GCMS.pdf EI MS Agilent 5973 MSD
10918-0428460-GCMS.pdf EI MS 3-epi-CP47,497-C8
10919-0428461-GCMS.pdf EI MS 3-epi-CP47,497
CP 47497-C8-homolog CCCC No. 10908.pdf SP-GC-IR Solid Phase IR
CP-47, 497 DMOH edit.pdf SP-GC-IR DiscovIR
Vendor ID URL
Cayman Chemical 10918 (3-epi) http://www.caymanchem.com/app/template/Product.vm/catalog/10918
Cayman Chemical 10908 https://www.caymanchem.com/app/template/Product.vm/catalog/10908
Toronto Research Chemicals H941620 https://www.trc-canada.com/detail.php?CatNum=H941620
Title Publication Date Vol. Iss. Page(s) Remarks
A new pyrazole-carboxamide type synthetic cannabinoid AB-CHFUPYCA [N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(cyclohexylmethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxamide] identified in illegal product Forensic Toxicology 2015-07-01 Vol 33 (367-373) Nahoko Uchiyama et al
Consideration of the major cannabinoid agonists 2009-07-00 Advisory Council on the Misuse of Drugs
Understanding the Spice phenomenon 2009-00-00 European Monitoring Centre for Drugs and Drug Addiction
Further consideration of the synthetic cannabinoids 2012-10-18 Advisory Council on the Misuse of Drugs
GC–MS and FTIR evaluation of the six benzoyl-substituted-1-pentylindoles: Isomeric synthetic cannabinoids Talanta 2014-11-01 Vol 129 (171-182) Forrest T. Smitha et al
Detection and identification of the new potential synthetic cannabinoids 1-pentyl-3-(2-iodobenzoyl)indole and 1-pentyl-3-(1-adamantoyl)indole in seized bulk powders in Hungary Forensic Science International 2012-01-01 Vol 214 (27-32) Péter Jankovics et al
Synthetic cannabinoids and cathinones: prevalence and markets Forensic Science Review 2013-03-01 Vol 25 (7-26) Bretteville-Jensen et al
Identification and analytical properties of new synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety Forensic Science International 2013-03-10 Vol 226 (62-73) Vadim Shevyrin et al
Spice, bath salts, and the U.S. military: the emergence of synthetic cannabinoid receptor agonists and cathinones in the U.S. Armed Forces. 2012-09-01 Loeffler G, Hurst D, Penn A, Yung K
Synthetic cannabinoid and marijuana exposures reported to poison centers Hum Exp Toxicol 2012-10-31 (1006-1011) MB Forrester et al
Separation and structural characterization of the synthetic cannabinoids JWH-412 and 1-[(5-fluoropentyl)-1H-indol-3yl]-(4-methylnaphthalen-1-yl)methanone using GC–MS, NMR analysis and a flash chromato Forensic Science International 2012-07-12 Vol 220 (e17-e22) Bjoern Moosmann et al
Cannabinoid chemistry: an overview Cannabinoids as Therapeutics 2005-01-01 (23-46) Lumír O. Hanuš and Raphael Mechoulam
- SCHEDULING UPDATE - [Synthetic Cannabinoids] Microgram Bulletin 2011-01-00 Vol 44 (1) Proposed Temporary Placement of Five Synthetic Cannabinoids Into Schedule I
Identification of a Cannabinoid Analog as a New Type of Designer Drug in a Herbal Product Chem. Pharm. Bull. 2009-04-00 Vol 57(4) Uchiyama et al.
Chemical Analysis of Synthetic Cannabinoids as Designer Drugs in Herbal Products For. Sci. Int. 2010-00-00 Vol 198 Uchiyama et al.
Use of High-Resolution Accurate Mass Spectrometry to Detect Reported and Previously Unreported Cannabinomimetics in J. Anal. Toxicol. 2010-06-00 Vol 34 Hudson et al.
JMS Letter: J. Mass Spectrom. 2009-00-00 Vol 44 Auwarter et al.
Isomeric analysis of synthetic cannabinoids detected as designer drugs. DOI: 10.1248/yakushi.131.1141 Yakugaku Zasshi 2011-01-01 Vol 131 (7) Uchiyama N, Kikura-Hanajiri R, Shoda T, Fukuhara K, Goda Y
Identification of Synthetic Cannabinoids in Herbal Incense Blends in the United States J. For. Sci. 2012-09-01 Vol 57 Barry K. Logan et al
Determination of the chemical composition of Spice aromatic smoking blends by chromatography-mass spectrometry J. Analytical Chem. 2011-12-01 Vol 66 (12) S. V. Nekhoroshev, V. P. Nekhoroshev, M. N. Remizova, A. V. Nekhorosheva
Identification of 1-butyl-3-(1-(4-methyl)naphtoyl)indole detected for the first time in “herbal high” products on the Italian market Forensic Science International 2012-11-30 Vol 223 (e42-e46) Ermanno Valoti et al
Database ID URL
Mass Spectra of Designer Drugs 2010
SWGDRUG Mass Spectral Library 527 http://www.swgdrug.org/ms.htm
SWGDRUG Monographs CP 47,497-C8 Homolog Monograph http://www.swgdrug.org/Monographs/CP%2047,497-C8-homolog.pdf
European Project Response to Challenges in Forensic Drug Analyses CP 47,497-C8 Homolog Monograph
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