Cannabicyclol

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]

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^N
PubChem CID	30607
ChemSpider	28407^Y
ChEMBL	ChEMBL154127^Y
CompTox Dashboard (EPA)	DTXSID70900962
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^Y Key:IGHTZQUIFGUJTG-UHFFFAOYSA-N^Y
^NY (what is this?)  (verify)

CBL is not scheduled under the Convention on Psychotropic Substances.

See also

• Cannabinoids
• Cannabis
• Medical cannabis

External links

• CTD's Cannabicyclol page from the Comparative Toxicogenomics Database
• Wiley-VCH list of chemicals

References

1. Dach, J.; Moore, E.A.; Kander, J. (2015). Cannabis Extracts in Medicine. McFarland. p. 78. Retrieved 28 May 2019.CS1 maint: multiple names: authors list (link)
2. ApSimon, J., ed. (2009). The Total Synthesis of Natural Products. John Wiley & Sons. pp. 229–30. Retrieved 28 May 2019.