1735-93-9

Upstream product

• 71-43-2 benzene 
• 1737-54-8 (3,4-Dichlor-heptafluorbutyl)-benzol 
• 2600-17-1 Heptafluor-4-phenyl-1-buten 

Downstream Products

• 14160-56-6 α,α,β,β-Tetrafluor-hydrocinnamonitril 
• 14160-55-5 α,α,β,β-Tetrafluor-hydrozimtsaeure-amid 
• 14160-57-7 α,α,β,β-Tetrafluor-hydrozimtsaeure-amidin 
• 17667-17-3 1,1,2,2-Tetrafluor-1-iod-2-(3-nitrophenyl)-ethan 
• 17667-14-0 1,1,2,2,3,3,4,4-Octafluor-1,4-bis-<3-nitro-phenyl>-butan 
• 5171-80-2 1,1,2,2,3,3,4,4-Octafluor-1,4-diphenyl-butan 
• 17667-15-1 1.1.2.2.3.3.4.4-Octafluor-1.4-bis-<3-amino-phenyl>-butan 
• 17667-11-7 1,1,2,2-tetrafluoro-1-iodo-2-phenylethane 
• 14160-54-4 ethyl 2,2,3,3-tetrafluoro-3-phenylpropanoate 

Relevant academic research and scientific papers

FLUORINE-CONTAINING COMPLEX COMPOUND, AND PRODUCTION METHOD FOR FLUORINE-CONTAINING ORGANIC COMPOUND EMPLOYING SAME

An object of the present invention is to enable the synthesis of various fluorine-containing compounds having an organic group at both terminals of their tetrafluoroethylene structure (—CF2—CF2—). The present invention provides a flu

Fluoroalkylcopper(I) complexes generated by the carbocupration of tetrafluoroethylene: Construction of a tetrafluoroethylene-bridging structure

We report a copper-mediated synthesis of a variety of 1,2-difunctionalized-1,1,2,2-tetrafluoroethylene derivatives via the carbocupration of tetrafluoroethylene. The key synthetic intermediates, 2-aryl-1,1,2,2-tetrafluoroethylcopper complexes, can be easily prepared, stored, and used as fluoroalkylation reagents. The molecular structure was unambiguously determined by X-ray crystallography and NMR analysis. We applied this method to the short-step synthesis of a liquid-crystalline compound bearing a tetrafluoroethylene-bridging structure.