Structure via PubChem · Public domain (PubChem)
cannabivarin
Sign in to saveAlso known as CBV
Cannabivarin (CBV), also known as cannabivarol, is considered a non-psychoactive cannabinoid — it does not produce the euphoric side effects found in THC. Minor amounts of CBV are found in the hemp plant Cannabis sativa. It is an analog of cannabinol (CBN) with the side chain shortened by two methylene bridges (). CBV is an oxidation product of tetrahydrocannabivarin (THCV, THV).
Chemical data
- Formula
- C19H22O2
- Molecular weight
- 282.4 g/mol
- IUPAC name
- 6,6,9-trimethyl-3-propylbenzo[c]chromen-1-ol
- SMILES
- CCCC1=CC(=C2C(=C1)OC(C3=C2C=C(C=C3)C)(C)C)O
- InChIKey
- SVTKBAIRFMXQQF-UHFFFAOYSA-N
- XLogP
- 5
- Polar surface area
- 29.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 282.16198
Show 4 more facts
- chemical formula
- C₁₉H₂₂O₂
- canonical SMILES
- CCCC1=CC2=C(C(=C1)O)C3=C(C=CC(=C3)C)C(O2)(C)C
- found in taxon
- Cannabis sativa
- Commons category
- Cannabivarin
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
6 sectionsContents
- Chemistry
- Legal status
- United States
- See also
- References
- External links
Cannabivarin (CBV), also known as cannabivarol, is considered a non-psychoactive cannabinoid — it does not produce the euphoric side effects found in THC. Minor amounts of CBV are found in the hemp plant Cannabis sativa. It is an analog of cannabinol (CBN) with the side chain shortened by two methylene bridges (). CBV is an oxidation product of tetrahydrocannabivarin (THCV, THV).
== Chemistry == It has no double bond isomers nor stereoisomers.
Excerpted from Wikipedia’s “cannabivarin” article, available under the CC BY-SA 4.0 licence.