Cannabivarin

Cannabivarin
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
CAS Number	33745-21-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	540898 ;
MeSH	cannabivarin
PubChem CID	622545;
CompTox Dashboard (EPA)	DTXSID00187421 ;
	InChI 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 Key: SVTKBAIRFMXQQF-UHFFFAOYSA-N ; 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;
	SMILES Oc2cc(cc1OC(c3c(c12)cc(cc3)C)(C)C)CCC;
Properties
Chemical formula	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).

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

It has no double bond isomers nor stereoisomers.

Legal status

It is not scheduled by Convention on Psychotropic Substances.

United States

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

^ 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.
^ §1308.11 Schedule I.

External links

Erowid Compounds found in Cannabis sativa

[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.

[PART_1308_—_SCHEDULES_OF_CONTROLLED_SUBSTANCES_-_1308.11_Schedule_I-2] §1308.11 Schedule I.

[1]

[2]