2-Isopropyl-5-methyl-1- (2,6-dihydroxy-1,2-dimethylheptylphenyl) cyclohex-1-en
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Structural formula without stereochemistry | ||||||||||
General | ||||||||||
Surname | 2-Isopropyl-5-methyl-1- (2,6-dihydroxy-1,2-dimethylheptylphenyl) cyclohex-1-en | |||||||||
Molecular formula | C 25 H 40 O 2 | |||||||||
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properties | ||||||||||
Molar mass | 372.58 g mol −1 | |||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
2-isopropyl-5-methyl-1- (2,6-dihydroxy-1,2-dimethylheptylphenyl) cyclohex-1-ene is an analgesic and a cannabinoid - agonist . It is chemically a ring-opened cannabinoid derivative and an analog of cannabidiol . Unlike cannabidiol, this compound has powerful cannabis-like effects , which is why it is believed to act as a CB 1 agonist.
It can be made from the 1,2-dimethylheptyl analog of cannabidiol by a Birch reduction .
Individual evidence
- ↑ see entry in Beilstein , accessed on March 15, 2012.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ Razdan, K .: The Total Synthesis of Cannabinoids . In: John Apsimon (Ed.): The Total Synthesis of Natural Products . Wiley Interscience, 1981, ISBN 978-0-471-05460-3 , p. 245.
- ^ Razdan RK, Pars HG, Thompson WR, Granchelli FE: Lithium-ammonia reduction of tetrahydrocannabinols . In: Tetrahedron Letters . 15, No. 49-50, 1974, p. 4315. doi : 10.1016 / S0040-4039 (01) 92152-5 .