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Cannabigerovarol

Base Information
  • Chemical Name:Cannabigerovarol
  • CAS No.:55824-11-8
  • Molecular Formula:C19H28O2
  • Molecular Weight:288.43
  • Hs Code.:
Cannabigerovarol

Synonyms:CBGV;CANNABIGEROVARIN;cannabigeroldivarin;cannabigerol propyl;

Suppliers and Price of Cannabigerovarol
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Cayman Chemical
  • Cannabigerovarin ≥98%
  • 5mg
  • $ 356.00
  • Cayman Chemical
  • Cannabigerovarin ≥98%
  • 1mg
  • $ 97.00
Total 9 raw suppliers
Chemical Property of Cannabigerovarol
Chemical Property:
  • Boiling Point:445.7±40.0 °C(Predicted) 
  • PKA:9.68±0.40(Predicted) 
  • PSA:40.46000 
  • Density:1.003±0.06 g/cm3(Predicted) 
  • LogP:5.28550 
Purity/Quality:

99% *data from raw suppliers

Cannabigerovarin ≥98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Cannabigerovarol

There total 7 articles about Cannabigerovarol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With toluene-4-sulfonic acid; In chloroform; at 20 ℃; for 12h; Darkness;
Guidance literature:
(E)-4-(3,7-dimethylocta-2,6-dienyl)-3,5-bis(trimethylsilyloxy)phenyl trifluoromethanesulfonate; propylzinc bromide; With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; at 20 ℃; for 15h; Inert atmosphere; Schlenk technique;
With sulfuric acid; water; In tetrahydrofuran; at 20 ℃; for 1h; Inert atmosphere; Schlenk technique;
Guidance literature:
Multi-step reaction with 4 steps
1.1: boron trifluoride diethyl etherate; silver nitrate; magnesium sulfate / acetonitrile / 4 h / 20 °C / Inert atmosphere; Schlenk technique
2.1: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere; Schlenk technique
3.1: triethylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere; Schlenk technique
4.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / tetrahydrofuran / 15 h / 20 °C / Inert atmosphere; Schlenk technique
4.2: 1 h / 20 °C / Inert atmosphere; Schlenk technique
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; boron trifluoride diethyl etherate; magnesium sulfate; silver nitrate; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile;
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