33745-21-0 Usage
Uses
Used in Pharmaceutical Research:
Cannabivarol is used as a research compound for studying its potential therapeutic effects and interactions with the endocannabinoid system. It may have potential applications in the development of new drugs and therapies for various medical conditions.
Used in Forensic Applications:
Cannabivarol is used as a forensic standard for the identification and quantification of cannabinoids in biological samples, such as blood, urine, or hair. This is crucial for legal and medical purposes, including drug testing and understanding the effects of cannabinoids on human health.
Used in Cannabis Industry:
Cannabivarol is used as a constituent in the development of cannabis products, such as oils, tinctures, and edibles. Its unique properties and potential therapeutic effects may contribute to the growing interest in the medicinal and recreational use of cannabis.
Check Digit Verification of cas no
The CAS Registry Mumber 33745-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,4 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33745-21:
(7*3)+(6*3)+(5*7)+(4*4)+(3*5)+(2*2)+(1*1)=110
110 % 10 = 0
So 33745-21-0 is a valid CAS Registry Number.
InChI: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
33745-21-0Relevant academic research and scientific papers
METHODS FOR SELECTIVE AROMATIZATION OF CANNABINOIDS
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Paragraph 0070-0072, (2022/02/11)
The present invention relates to methods of selective aromatization of cannabinoids. Such methods may be used, among other purposes, for the removal of delta-9-tetrahydrocannabinol from hemp extracts or other samples by selectively converting delta-9-tetrahydrocannabinol to cannabinol using ortho-quinone catalysts.
One-Pot Total Synthesis of Cannabinol via Iodine-Mediated Deconstructive Annulation
Caprioglio, Diego,Mattoteia, Daiana,Minassi, Alberto,Pollastro, Federica,Lopatriello, Annalisa,Muňoz, Eduardo,Taglialatela-Scafati, Orazio,Appendino, Giovanni
, p. 6122 - 6125 (2019/08/20)
The thermal degradation of cannabichromene (CBC, 3) is dominated by cationic reactions and not by the pericyclic rearrangements observed in model compounds. The rationalization of these differences inspired the development of a process that coupled, in an aromatization-driven single operational step, the condensation of citral and alkylresorciniols to homoprenylchromenes and their in situ deconstructive annulation to benzo[c]chromenes. This process was applied to a total synthesis of cannabinol (CBN, 5) and to its molecular editing.
