Introduction of CAS:376-90-9 | 2,2,3,3,4,4-HEXAFLUORO-1,5-PENTANEDIOL
2,2,3,3,4,4-Hexafluoro-1,5-pentanediol is a fluorinated building block with the linear formula HOCH2(CF2)3CH2OH . It has a molecular weight of 212.09 . This compound is used for the preparation of cyclic and acyclic polyfluorosiloxanes as precursors to per- and polyfluoroethers.
Specification of CAS:376-90-9 | 2,2,3,3,4,4-HEXAFLUORO-1,5-PENTANEDIOL
|
ITEMS |
SPECIFICATION |
|
Purity |
98% |
|
BOiling point |
111.5 °C10 mm Hg(lit.) |
|
Density |
1.4048 (estimate) |
|
Form |
powder to crystal |
|
Color |
White to Almost white |
Research Application of CAS:376-90-9 | 2,2,3,3,4,4-HEXAFLUORO-1,5-PENTANEDIOL
Synthesis of Organometallic Compounds, Catalysts, and Materials for Fuel Cells
2,2,3,3,4,4-Hexafluoro-1,5-pentanediol is used in the synthesis of organometallic compounds, catalysts, and materials for fuel cells .The outcomes would also depend on the specific synthesis process. The source does not provide any quantitative data or statistical analyses .
Preparation of Cyclic and Acyclic Polyfluorosiloxanes
2,2,3,3,4,4-Hexafluoro-1,5-pentanediol is used for the preparation of cyclic and acyclic polyfluorosiloxanes as precursors to per- and polyfluoroethers .
The outcomes would also depend on the specific synthesis process. The source does not provide any quantitative data or statistical analyses .
One-Pot Production of 1,5-Pentanediol from Furfural
2,2,3,3,4,4-Hexafluoro-1,5-pentanediol is used in the one-pot production of 1,5-pentanediol (1,5-PDO) from sustainable sources such as furfural . This is a key reaction to compete with existing fossil sources . The productivity is maximized when Co 2+ species partially substitute Mg 2+ species in parent LDH, yielding promising pentanediol yields under mild reaction conditions .
Preparation of Polyesters and Polyurethanes
2,2,3,3,4,4-Hexafluoro-1,5-pentanediol is used for the preparation of polyesters and polyurethanes . It allows the manufacture of these polymers via a more economic and sustainable pathway than analogues, such as 1,4-butanediol and 1,6-hexanediol .The outcomes would also depend on the specific synthesis process. The source does not provide any quantitative data or statistical analyses .
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