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2-(2-Phenylethenyl)furan

Base Information Edit
  • Chemical Name:2-(2-Phenylethenyl)furan
  • CAS No.:1202-49-9
  • Molecular Formula:C12H10O
  • Molecular Weight:170.211
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50709910
  • Mol file:1202-49-9.mol
2-(2-Phenylethenyl)furan

Synonyms:2-(2-Phenylethenyl)furan;styrylfuran;SCHEMBL8807020;DTXSID50709910

Suppliers and Price of 2-(2-Phenylethenyl)furan
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
Total 1 raw suppliers
Chemical Property of 2-(2-Phenylethenyl)furan Edit
Chemical Property:
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:170.073164938
  • Heavy Atom Count:13
  • Complexity:168
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C=CC2=CC=CO2
Technology Process of 2-(2-Phenylethenyl)furan

There total 73 articles about 2-(2-Phenylethenyl)furan 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 15-crown-5; sodium hydride; In tetrahydrofuran; at 0 - 25 ℃; for 6h;
DOI:10.1055/s-1981-29351
Guidance literature:
With potassium carbonate; In ethanol; chloroform; at 60 ℃; under 75007.5 Torr; Overall yield = 93 percent; Overall yield = 0.03 g; stereoselective reaction; Flow reactor;
DOI:10.1002/ejoc.202100761
Guidance literature:
With potassium carbonate; In ethanol; Milling;
DOI:10.1039/c2gc35669d
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