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9,10-Difluoroanthracene

Base Information
  • Chemical Name:9,10-Difluoroanthracene
  • CAS No.:1545-69-3
  • Molecular Formula:C14H8F2
  • Molecular Weight:214.214
  • Hs Code.:
  • Mol file:1545-69-3.mol
9,10-Difluoroanthracene

Synonyms:9,10-Difluoranthracen;9,10-difluoro-anthracene;9,10-Difluoroanthracen;9,10-Difluor-anthracen;

Suppliers and Price of 9,10-Difluoroanthracene
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
Total 7 raw suppliers
Chemical Property of 9,10-Difluoroanthracene
Chemical Property:
  • PSA:0.00000 
  • LogP:4.27120 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 9,10-Difluoroanthracene

There total 9 articles about 9,10-Difluoroanthracene 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 N-fluoropyridinium triflate; In 1,2-dichloro-ethane; for 5h; Heating;
DOI:10.1021/jo00266a006
Guidance literature:
Multi-step reaction with 2 steps
1: 65 percent / DDQ / benzene / 14 h / 140 °C
2: 24 percent / N-fluoropyridinium triflate (33) / 1,2-dichloro-ethane / 5 h / Heating
With N-fluoropyridinium triflate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,2-dichloro-ethane; benzene;
DOI:10.1021/jo00266a006
Guidance literature:
With n-butyllithium; N-fluoro-N-(tert-butyl)benzenesulfonamide; Yield given. Multistep reaction; 1.) ether, 10 min, 2.) ether, from -78 deg C to RT;
DOI:10.1021/jo00244a056
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