CAS 21366-63-2: Cannabicyclol
Description:Cannabicyclol (CBL) is a lesser-known cannabinoid derived from the cannabis plant, specifically formed through the degradation of tetrahydrocannabinol (THC). It is characterized by its unique bicyclic structure, which distinguishes it from other cannabinoids. CBL is non-psychoactive, meaning it does not produce the euphoric effects commonly associated with THC. This compound is believed to possess potential therapeutic properties, although research on its pharmacological effects is still limited. CBL is typically found in trace amounts in cannabis strains and can be isolated through various extraction and purification methods. Its chemical structure includes a series of carbon rings, contributing to its stability and interaction with the endocannabinoid system, albeit in a different manner than more prevalent cannabinoids like CBD and THC. As interest in cannabinoids continues to grow, CBL may offer insights into the diverse effects and benefits of cannabis compounds, warranting further investigation into its potential applications in medicine and wellness.
Formula:C21H30O2
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/t14-,18+,19+,21+/m0/s1
InChI key:InChIKey=IGHTZQUIFGUJTG-QSMXQIJUSA-N
SMILES:OC=1C=C(C=C2OC3(C)CCC4C3C(C12)C4(C)C)CCCCC
- Synonyms:
- (1aS,3aR,8bR,8cR)-1a,2,3,3a,8b,8c-Hexahydro-1,1,3a-trimethyl-6-pentyl-1H-4-oxabenzo[f]cyclobut[cd]inden-8-ol
- 1H-4-Oxabenzo[f]cyclobut[cd]inden-8-ol, 1a,2,3,3a,8b,8c-hexahydro-1,1,3a-trimethyl-6-pentyl-, (1aS,3aR,8bR,8cR)-
- 1H-4-Oxabenzo[f]cyclobut[cd]inden-8-ol, 1a,2,3,3a,8b,8c-hexahydro-1,1,3a-trimethyl-6-pentyl-, [1aS-(1aα,3aα,8bα,8cα)]-
- 1H-4-Oxabenzo[f]cyclobut[cd]inden-8-ol, 1aα,2,3,3a,8bα,8cα-hexahydro-1,1,3a-trimethyl-6-pentyl-
- 1H-4-oxabenzo[f]cyclobut[cd]inden-8-ol, 1a,2,3,3a,8b,8c-hexahydro-1,1,3a-trimethyl-6-pentyl-
- Cannabicyclol
- Cannabipinol
- Pentylcannabicyclol
