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Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI)

Base Information
  • Chemical Name:Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI)
  • CAS No.:2991-99-3
  • Molecular Formula:C6H4 F2 O S
  • Molecular Weight:162.1571664
  • Hs Code.:
  • Mol file:2991-99-3.mol
Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI)

Synonyms:Ketone,difluoromethyl 2-thienyl (6CI,8CI)

Suppliers and Price of Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI)
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
  • Rieke Metals
  • 2,2-Difluoro-1-thiophen-2-yl-ethanone
  • 5g
  • $ 1728.00
  • Abosyn
  • 2,2-difluoro-1-(thiophen-2-yl)ethanone 95%-98%
  • 1g
  • $ 440.00
Total 6 raw suppliers
Chemical Property of Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI)
Chemical Property:
  • Boiling Point:77 - 80 °C (11 mmHg) 
  • PSA:45.31000 
  • LogP:2.19590 
Purity/Quality:

99% *data from raw suppliers

2,2-Difluoro-1-thiophen-2-yl-ethanone *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI)

There total 16 articles about Ethanone, 2,2-difluoro-1-(2-thienyl)- (9CI) 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:
1,1,1-trifluoro-4-(2-thienyl)butane-2,4-dione; With Selectfluor; In acetonitrile; at 90 ℃; for 3h; Inert atmosphere;
With water; In acetonitrile; for 0.25h; Inert atmosphere; Reflux;
With triethylamine; In acetonitrile; at 20 ℃; for 16h; regioselective reaction; Inert atmosphere;
DOI:10.1039/c5ob02468d
Guidance literature:
With triethylamine; In acetonitrile; at 20 ℃; for 24h; regioselective reaction; Inert atmosphere;
DOI:10.1039/c5ob02468d
Guidance literature:
With hydrogen; In ethanol; at 70 ℃;
DOI:10.1002/ejoc.201701322
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