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1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane

Base Information Edit
  • Chemical Name:1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane
  • CAS No.:35207-97-7
  • Molecular Formula:C8H8F8
  • Molecular Weight:256.139
  • Hs Code.:
  • Mol file:35207-97-7.mol
1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane

Synonyms:

Suppliers and Price of 1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane Edit
Chemical Property:
  • Boiling Point:137.9±35.0 °C(Predicted) 
  • Density:1.37±0.1 g/cm3(Predicted) 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:
Useful:
Technology Process of 1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane

There total 3 articles about 1,1,2,2-Tetrafluoro-3-(1,1,2,2-tetrafluorobutyl)cyclobutane 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 hydrogen; nickel; In ethanol; at 25 ℃; for 3h; under 53200 Torr;
DOI:10.1039/j39710003894
Guidance literature:
Multi-step reaction with 2 steps
1: menth-1-en-8-ol / 14 h / 220 °C
2: H2 / Raney-Ni / ethanol / 3 h / 25 °C / 53200 Torr
With terpineol; hydrogen; nickel; In ethanol;
DOI:10.1039/j39710003894
Guidance literature:
Multi-step reaction with 3 steps
1: KOH / ethane-1,2-diol / 120 °C
2: menth-1-en-8-ol / 14 h / 220 °C
3: H2 / Raney-Ni / ethanol / 3 h / 25 °C / 53200 Torr
With potassium hydroxide; terpineol; hydrogen; nickel; In ethanol; ethylene glycol;
DOI:10.1039/j39710003894
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