Cannabicyclol

Cannabicyclol
Clinical data
ATC code	none;
Legal status
Legal status	UN: Unscheduled;
Identifiers
	IUPAC name (1aR-(1a alpha,3a alpha,8b alpha,8c alpha))-1a,2,3,3a,8b,8c-hexahydro-1,1,3a-trimethyl-6-pentyl-1H-4-oxabenzo(f)cyclobut(cd)inden-8-ol;
CAS Number	21366-63-2 ;
PubChem CID	30607;
ChemSpider	28407 ;
UNII	MP5WZK8M5U;
ChEMBL	ChEMBL154127 ;
CompTox Dashboard (EPA)	DTXSID301356075 DTXSID70900962, DTXSID301356075 ;
Chemical and physical data
Formula	C21H30O2
Molar mass	314.469 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES Oc4c1c(OC3(C2C1C(C2CC3)(C)C)C)cc(c4)CCCCC;
	InChI InChI=1S/C21H30O2/c1-5-6-7-8-13-11-15(22)17-16(12-13)23-21(4)10-9-14-18(21)19(17)20(14,2)3/h11-12,14,18-19,22H,5-10H2,1-4H3 ; Key:IGHTZQUIFGUJTG-UHFFFAOYSA-N ;
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Cannabicyclol (CBL) is a non-psychoactive cannabinoid found in Cannabis. CBL is a degradative product like cannabinol, with cannabichromene degrading into CBL through natural irradiation^[1] or under acid conditions.^[2]

CBL is not scheduled under the Convention on Psychotropic Substances.

References

^ Dach J, Moore EA, Kander J (2015). Cannabis Extracts in Medicine. McFarland. p. 78. ISBN 9781476621111. Retrieved 28 May 2019.
^ ApSimon J, ed. (2009). The Total Synthesis of Natural Products. John Wiley & Sons. pp. 229–30. ISBN 9780470129531. Retrieved 28 May 2019.

External links

CTD's Cannabicyclol page from the Comparative Toxicogenomics Database
Wiley-VCH list of chemicals Archived 2007-09-27 at the Wayback Machine

[DachCanna15-1] Dach J, Moore EA, Kander J (2015). Cannabis Extracts in Medicine. McFarland. p. 78. ISBN 9781476621111. Retrieved 28 May 2019.

[ApSimonTheTotal09-2] ApSimon J, ed. (2009). The Total Synthesis of Natural Products. John Wiley & Sons. pp. 229–30. ISBN 9780470129531. Retrieved 28 May 2019.

[1]

[2]

See also

References

External links