(C9)-CP 47,497

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(C9)-CP 47,497
(C9)-CP 47,497 Structure.svg
Legal status
Legal status
  • DE: Anlage II (Authorized trade only, not prescriptible)
  • UK: Class B
  • Illegal in France
Identifiers
IUPAC name
  • 2-[(1S,3R)-3-hydroxycyclohexyl]-5-(2-methyldecan-2-yl)phenol
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC23H38O2
Molar mass346.555 g·mol−1
3D model (JSmol)
SMILES
  • OC1=CC(C(C)(C)CCCCCCCC)=CC=C1[C@@H]2C[C@H](O)CCC2
InChI
  • InChI=1S/C23H38O2/c1-4-5-6-7-8-9-15-23(2,3)19-13-14-21(22(25)17-19)18-11-10-12-20(24)16-18/h13-14,17-18,20,24-25H,4-12,15-16H2,1-3H3/t18-,20+/m0/s1
  • Key:BIGNODGYJZJTBM-AZUAARDMSA-N

(C9)-CP 47,497 (CP 47,497 dimethylnonyl homologue) is a synthetic cannabinoid, a CP 47,497 homologue.[1]

Its systematic name is 2-[(1S,3R)-3-hydroxycyclohexyl]-5-(1,1-dimethylnonyl)phenol.

See also[]

  • Synthetic cannabis
  • (C6)-CP 47,497
  • (C7)-CP 47,497 (CP 47,497 itself)
  • (C8)-CP 47,497

References[]

  1. ^ Helander A (January 2017). "Synthetic Cannabinoid Receptor Agonists (Spice) as New Recreational Psychoactive Substances.". In Preedy VR (ed.). Handbook of Cannabis and Related Pathologies. London, United Kingdom: Academic Press. pp. 839-847 (843). ISBN 978-0-12-800827-0.
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