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rac-Falcarinol

Base Information
  • Chemical Name:rac-Falcarinol
  • CAS No.:4117-12-8
  • Molecular Formula:C17H24O
  • Molecular Weight:244.377
  • Hs Code.:2905290000
  • Mol file:4117-12-8.mol
rac-Falcarinol

Synonyms:(9Z)-heptadeca-1,9-dien-4,6-diyn-3-ol;

Suppliers and Price of rac-Falcarinol
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
  • TRC
  • rac-Falcarinol
  • 50mg
  • $ 7505.00
  • American Custom Chemicals Corporation
  • RAC-FALCARINOL 95.00%
  • 5MG
  • $ 457.85
Total 7 raw suppliers
Chemical Property of rac-Falcarinol
Chemical Property:
  • PSA:20.23000 
  • LogP:3.84690 
  • Storage Temp.:Amber Vial, -86°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
Purity/Quality:

95% *data from raw suppliers

rac-Falcarinol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Falcarinol is a covalent cannabinoid CB1 receptor antagonist and induces pro-allergic effects in skin. A natural pesticide produced by carrots and red ginseng, protecting hosts roots from various fungal diseases. It has been shown to have nutritional benefits, reducing the risk of developing specific forms of cancer.
Technology Process of rac-Falcarinol

There total 9 articles about rac-Falcarinol 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:
rac-hept-1-ene-4,6-diyn-3-ol; With copper(l) iodide; tetraethylammonium chloride; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;
(Z)-1-chlorodec-2-ene; In N,N-dimethyl-formamide; at 20 ℃; for 8h; optical yield given as %de;
DOI:10.1016/j.tet.2010.10.049
Guidance literature:
With copper(l) iodide; tetraethylammonium chloride; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 1h; optical yield given as %de;
DOI:10.1016/j.tet.2010.10.049
Guidance literature:
Multi-step reaction with 4 steps
1: (i) LiNH2, liq. NH3, (ii) /BRN= 1697160/, (iii) aq. H2SO4
2: H2 / Lindlar catalyst
3: (i) TsCl, (ii) /BRN= 969224/
4: NH2OH*HCl, CuCl, EtNH2
With hydroxylamine hydrochloride; hydrogen; ethylamine; copper(l) chloride; Lindlar's catalyst;
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