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cannabicyclohexanol

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cannabicyclohexanol

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Cannabicyclohexanol (CCH, CP 47,497 dimethyloctyl homologue, (C8)-CP 47,497) is a cannabinoid receptor agonist drug, developed by Pfizer in 1979. On 19 January 2009, the University of Freiburg in Germany announced that an analog of CP 47,497 was the main active ingredient in the herbal incense product Spice, specifically the 1,1-dimethyloctyl homologue of CP 47,497, which is now known as cannabicyclohexanol. The 1,1-dimethyloctyl homologue of CP 47,497 is in fact several times more potent than the parent compound, which is somewhat unexpected as the 1,1-dimethylheptyl is the most potent substi

Chemical data

Formula
C22H36O2
Molecular weight
332.5 g/mol
IUPAC name
2-(3-hydroxycyclohexyl)-5-(2-methylnonan-2-yl)phenol
SMILES
CCCCCCCC(C)(C)C1=CC(=C(C=C1)C2CCCC(C2)O)O
InChIKey
HNMJDLVMIUDJNH-UHFFFAOYSA-N
XLogP
7.2
Polar surface area
40.5 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Wikidata facts

Subclass of
alcohols
Mass
332.271530392
Show 3 more facts
chemical formula
C₂₂H₃₆O₂
isomeric SMILES
CCCCCCCC(C)(C)c1ccc(c(c1)O)[C@@H]2CCC[C@@H](C2)O
canonical SMILES
CCCCCCCC(C)(C)c1ccc(C2CCCC(O)C2)c(O)c1
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Encyclopedic overview

7 sections
Contents
  • Enantiomers
  • Toxicity
  • Legal status
  • United States
  • Vermont
  • See also
  • References

Cannabicyclohexanol (CCH, CP 47,497 dimethyloctyl homologue, (C8)-CP 47,497) is a cannabinoid receptor agonist drug, developed by Pfizer in 1979. On 19 January 2009, the University of Freiburg in Germany announced that an analog of CP 47,497 was the main active ingredient in the herbal incense product Spice, specifically the 1,1-dimethyloctyl homologue of CP 47,497, which is now known as cannabicyclohexanol. The 1,1-dimethyloctyl homologue of CP 47,497 is in fact several times more potent than the parent compound, which is somewhat unexpected as the 1,1-dimethylheptyl is the most potent substituent in classical cannabinoid compounds such as HU-210.

==Enantiomers== Cannabicyclohexanol has four enantiomers, which by analogy with other related cannabinoid compounds can be expected to have widely varying affinity for cannabinoid receptors, and consequently will show considerable variation in potency. While the (-)-cis enantiomer (-)-cannabicyclohexanol discovered in the original Pfizer research is expected to be the most potent, all four enantiomers have been isolated from illicit samples of this compound, and the properties of the other three enantiomers have not been studied in detail. Most commonly cannabicyclohexanol is encountered as a diastereomeric mix of the two cis or two trans isomers in varying ratios, though more rarely a mixture of all four enantiomers has been seen, as well as reasonably enantiopure samples of the most active isomer. Confusion can arise around the naming of these compounds as they can be viewed either as substituted phenols or substituted cyclohexanols, but this results in different numbering of the rings. Consequently, the active isomer can be named either 2-[(1S,3R)-3-hydroxycyclohexyl]-5-(2-methylnonan-2-yl)phenol or (1R,3S)-3-[2-hydroxy-4-(2-methylnonan-2-yl)phenyl]cyclohexan-1-ol. 300px|thumb|left|The four enantiomers of cannabicyclohexanol

Excerpted from Wikipedia’s “cannabicyclohexanol” article, available under the CC BY-SA 4.0 licence.

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