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1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene

Base Information Edit
  • Chemical Name:1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene
  • CAS No.:1091626-77-5
  • Molecular Formula:C19H16O
  • Molecular Weight:260.335
  • Hs Code.:
  • Mol file:1091626-77-5.mol
1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene

Synonyms:

Suppliers and Price of 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene
Supply Marketing:Edit
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
  • 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene
  • 25mg
  • $ 945.00
  • Medical Isotopes, Inc.
  • 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene
  • 25 mg
  • $ 2000.00
Total 5 raw suppliers
Chemical Property of 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene Edit
Chemical Property:
  • Melting Point:80-82oC 
  • Boiling Point:447.4±24.0 °C(Predicted) 
  • Density:1.117±0.06 g/cm3(Predicted) 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated) 
Purity/Quality:

99% *data from raw suppliers

1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene is an impurity of the selective serotonin reuptake inhibitor Dapoxetine (D185700).
Technology Process of 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene

There total 4 articles about 1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene 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 sodium hydroxide; In tetrahydrofuran; for 5h; Ambient temperature;
DOI:10.1080/00397919308012585
Guidance literature:
With potassium carbonate; In acetone; at 60 ℃; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.joc.6b02902
Guidance literature:
With potassium carbonate; potassium iodide; In acetone; Inert atmosphere; Reflux;
upstream raw materials:

α-naphthol

Cinnamyl bromide

cinnamyl chloride

Downstream raw materials:

α-naphthol

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