Chemistry:Abeo-HHC acetate
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Short description: Semi-synthetic THC derivative compound
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Identifiers | |
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Chemical and physical data | |
Formula | C23H34O3 |
Molar mass | 358.522 g·mol−1 |
3D model (JSmol) | |
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abeo-HHC acetate is a is a semi-synthetic derivative of tetrahydrocannabinol, first described in the 1980s. It is synthesised from the acetate ester of Delta-11-Tetrahydrocannabinol, which can be made to undergo a ring expansion reaction via a hydrazone intermediate to form abeo-HHC acetate.[1][2] It is structurally similar to HHC-acetate except it's substituted with a cycloheptyl ring instead of a cyclohexyl ring.
See also
References
- ↑ "Reactions of cannabinoid tosylhydrazones: Stereochemical aspects.". Tetrahedron 40 (19): 3839–3843. 1984. doi:10.1016/S0040-4020(01)88815-3.
- ↑ "Hexahydrocannabinol and closely related semi-synthetic cannabinoids: A comprehensive review". Drug Testing and Analysis. June 2023. doi:10.1002/dta.3519. PMID 37269160.
![]() | Original source: https://en.wikipedia.org/wiki/Abeo-HHC acetate.
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