Cannabivarin

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Cannabivarin
Cannabivarin.svg
Cannabivarin molecule ball.png
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
3D model (JSmol)
ChemSpider
MeSH cannabivarin
  • InChI=1S/C19H22O2/c1-5-6-13-10-16(20)18-14-9-12(2)7-8-15(14)19(3,4)21-17(18)11-13/h7-11,20H,5-6H2,1-4H3 checkY
    Key: SVTKBAIRFMXQQF-UHFFFAOYSA-N checkY
  • InChI=1/C19H22O2/c1-5-6-13-10-16(20)18-14-9-12(2)7-8-15(14)19(3,4)21-17(18)11-13/h7-11,20H,5-6H2,1-4H3
    Key: SVTKBAIRFMXQQF-UHFFFAOYAK
  • Oc2cc(cc1OC(c3c(c12)cc(cc3)C)(C)C)CCC
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).
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Infobox references

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 (-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]

  1. ^ 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. CiteSeerX 10.1.1.689.8592. doi:10.1002/jps.2600641033. PMID 1185546.
  2. ^ §1308.11 Schedule I.

See also[edit]

External links[edit]

  • Erowid Compounds found in Cannabis sativa