Δ-10-Tetrahydrocannabinol

In today's world, Δ-10-Tetrahydrocannabinol is a highly relevant topic that has captured the attention of millions of people around the world. With a significant impact on various aspects of daily life, Δ-10-Tetrahydrocannabinol has been the subject of debate and discussion in all spheres of society. From its impact on health and well-being, to its influence on economics and politics, Δ-10-Tetrahydrocannabinol has become a point of interest and concern for many. In this article, we will explore the phenomenon of Δ-10-Tetrahydrocannabinol in depth, analyzing its implications and consequences in different contexts. With a global perspective, we seek to shed light on this topic and provide a broader and more complete vision of its scope and importance in today's world.

Δ-10-Tetrahydrocannabinol
Identifiers
  • 6,6,9-trimethyl-3-pentyl-6a,7,8,9-tetrahydrobenzochromen-1-ol
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
Chemical and physical data
FormulaC21H30O2
Molar mass314.469 g·mol−1
3D model (JSmol)
  • CCCCCC1=CC(=C2C3=CC(CCC3C(OC2=C1)(C)C)C)O
  • InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h11-14,17,22H,5-10H2,1-4H3
  • Key:YLTWYAXWDLZZCU-UHFFFAOYSA-N

Δ-10-Tetrahydrocannabinol (Delta-10-THC, Δ10-THC, alternatively numbered as Δ2-THC) is a positional isomer of tetrahydrocannabinol, discovered in the 1980s. Two epimers have been reported in the literature, with the 9-methyl group in either the (R) or (S) conformation; of these, the (R) epimer appears to be the more active isomer as well as the double bond in the 10th position instead of the 9th maintaining about 30 to 40 percent the potency of delta-9-THC.[1][2][3] Δ10-THC has rarely been reported as a trace component of natural cannabis, though it is thought to be a degradation product similar to cannabinol rather than being produced by the plant directly. However, it is found more commonly as an impurity in synthetic delta-8-THC produced from cannabidiol[4][5][6] and can also be synthesized directly from delta-9-THC.[7]

See also

References

  1. ^ Srebnik M, Lander N, Breuer A, Mechoulam R (1984). "Base-catalysed double-bond isomerizations of cannabinoids: structural and stereochemical aspects". Journal of the Chemical Society, Perkin Transactions 1: 2881–6. doi:10.1039/P19840002881.
  2. ^ Järbe TU, Hiltunen AJ, Mechoulam R, Srebnik M, Breuer A (November 1988). "Separation of the discriminative stimulus effects of stereoisomers of delta 2- and delta 3-tetrahydrocannabinols in pigeons". European Journal of Pharmacology. 156 (3): 361–6. doi:10.1016/0014-2999(88)90281-6. PMID 2850933.
  3. ^ WHO Expert Committee on Drug Dependence Critical Review. Isomers of THC (PDF) (Report). World Health Organization. 2018.
  4. ^ Hanuš LO, Meyer SM, Muñoz E, Taglialatela-Scafati O, Appendino G (November 2016). "Phytocannabinoids: a unified critical inventory". Natural Product Reports. 33 (12): 1357–1392. doi:10.1039/c6np00074f. PMID 27722705.
  5. ^ Chan-Hosokawa A, Nguyen L, Lattanzio N, Adams WR (March 2021). "Emergence of Delta-8 Tetrahydrocannabinol (THC) in DUID Investigation Casework: Method Development, Validation and Application". Journal of Analytical Toxicology. 46 (1): 1–9. doi:10.1093/jat/bkab029. PMID 33754645.
  6. ^ Erickson BE. Delta-8-THC craze concerns chemists. Chemical & Engineering News, 30 August 2021
  7. ^ WO 2020248059, Adair C, Geiling B, Haghdoost Manjili M., "Methods for preparing cannabinoids by base-promoted double-bond migration.", published 2020-12-17, assigned to Canopy Growth Corporation 
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