Cannabivarin
From Wikipedia, the free encyclopedia
 |
|
 |
|
| Names | |
|---|---|
| Preferred IUPAC name
6,6,9-Trimethyl-3-propyl-6H-dibenzo[b,d]pyran-1-ol
|
|
| Other names
6,6,9-Trimethyl-3-propyl-6H-benzo[c]chromen-1-ol
|
|
| Identifiers | |
33745-21-0  |
|
| 3D model (Jmol) | Interactive image |
| ChemSpider | 540898 |
| MeSH | cannabivarin |
| PubChem | 622545 |
|
|
|
|
| Properties | |
| C19H22O2 | |
| Molar mass | 282.38 g/mol |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
 verify (what is  ?) |
|
| Infobox references | |
Cannabivarin, also known as cannabivarol or CBV, is a non-psychoactive cannabinoid found in minor amounts in the hemp plant Cannabis sativa. It is an analog of cannabinol (CBN) with the side chain shortened by two methylene bridges (-CH2-). CBV is an oxidation product of tetrahydrocannabivarin (THCV, THV).[1]
Chemistry[edit]
It has no double bond isomers nor stereoisomers.
Legal status[edit]
It is not scheduled by Convention on Psychotropic Substances.
United States[edit]
CBV is not scheduled at the federal level in the United States,[2] but it could be considered an analog (of THC), in which case, sales or possession intended for human consumption could be prosecuted under the Federal Analog Act.
References[edit]
- ^ Keith Bailey, Denise Gagné (October 1975). "Distinction of synthetic cannabidiol, cannabichromene, and cannabivarin by GLC using on-column methylation". Journal of Pharmaceutical Sciences. 64 (10): 1719–1720. doi:10.1002/jps.2600641033.
- ^ §1308.11 Schedule I.
See also[edit]
External links[edit]
- Erowid Compounds found in Cannabis sativa
 |
This cannabinoid related article is a stub. You can help Wikipedia by expanding it. |
