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(E,E)-Farnesol Benzyl Ether

Base Information
  • Chemical Name:(E,E)-Farnesol Benzyl Ether
  • CAS No.:56506-81-1
  • Molecular Formula:C22H32O
  • Molecular Weight:312.495
  • Hs Code.:
  • Mol file:56506-81-1.mol
(E,E)-Farnesol Benzyl Ether

Synonyms:(2E,6E)-1-(benzyloxy)-3,7,11-trimethyl-2,6,10-dodecatriene

Suppliers and Price of (E,E)-Farnesol Benzyl Ether
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
  • (E,E)-FarnesolBenzylEther
  • 50mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • (E,E)-FarnesolBenzylEther
  • 50 mg
  • $ 650.00
Total 1 raw suppliers
Chemical Property of (E,E)-Farnesol Benzyl Ether
Chemical Property:
  • Storage Temp.:Amber Vial, -20°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform, Dichloromethane, Ethyl Acetate, Methanol 
Purity/Quality:

(E,E)-FarnesolBenzylEther *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (E,E)-Farnesol Benzyl Ether is a Terpene derivative, used in the preparation of coenzymes Q, vitamin K and polyprenylquinones.
Technology Process of (E,E)-Farnesol Benzyl Ether

There total 5 articles about (E,E)-Farnesol Benzyl Ether 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:
Farnesol; With sodium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 2h;
benzyl chloride; In dimethyl sulfoxide; at 20 ℃; for 12h; Further stages.;
DOI:10.1039/b008104n
Guidance literature:
With lithium biphenylide; barium(II) iodide; Yield given. Multistep reaction; 1.) THF, -78 deg C, 20 min, 2.) THF, -78 deg C, 1 h;
DOI:10.1246/bcsj.68.1263
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