1767-94-8 Usage
Uses
Used in Specialty Polymers Production:
6H-PERFLUORO-1-HEXENE is used as a monomer in the production of specialty polymers for its unique properties, such as high thermal and chemical stability, and resistance to harsh conditions.
Used in Surfactants Production:
6H-PERFLUORO-1-HEXENE is used as a building block in the synthesis of surfactants, which are compounds that lower the surface tension between two liquids or a liquid and a solid.
Used in Advanced Materials Production:
6H-PERFLUORO-1-HEXENE is used in the production of advanced materials due to its unique properties, such as high thermal and chemical stability, and resistance to harsh conditions.
Used in Fluorochemicals Synthesis:
6H-PERFLUORO-1-HEXENE is used as a building block in the synthesis of fluorochemicals, which are compounds containing fluorine atoms and are used in various industrial applications.
Used in Industrial Applications:
6H-PERFLUORO-1-HEXENE is used in various industrial applications where fluorinated compounds are required, such as in the production of specialty polymers, surfactants, and other advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1767-94-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1767-94:
(6*1)+(5*7)+(4*6)+(3*7)+(2*9)+(1*4)=108
108 % 10 = 8
So 1767-94-8 is a valid CAS Registry Number.
InChI:InChI=1/C6HF11/c7-1(2(8)9)4(12,13)6(16,17)5(14,15)3(10)11/h3H
1767-94-8Relevant academic research and scientific papers
Coupling reactions of chlorofluoro and perfluoroalkyl iodides
Wlassics, Ivan,Tortelli, Vito
scheme or table, p. 1719 - 1728 (2009/06/05)
Coupling reactions of chlorofluoro- and perfluoroalkyl iodides R f-I with Rf = ClCF2CFCl-(CF2) 3CF2-, ClCF2CFClO(CF2) 3CF2-, ClCF2CFCl-, (CF3) 2CF- , (CF3)2CFCF2CF2- in the presence of a zinc/solvent system give dimers in good yields. Both homodimerizations (one iodide) and heterodimerizations (two different iodides) have been studied. The effect of temperature and solvent is shown. The zinc mediated dechlorination of vicinal chlorine atoms in the dimers afforded terminal alkenes and dienes.
