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Home  > 3-[2-(Perfluorohexyl)ethoxy]-1,2-epoxypropane

AA55407

122193-68-4 | 3-[2-(Perfluorohexyl)ethoxy]-1,2-epoxypropane

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $16.00 $11.00 -   +
1g 96% in stock $30.00 $21.00 -   +
5g 96% in stock $83.00 $58.00 -   +
25g 96% in stock $372.00 $260.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA55407
Chemical Name: 3-[2-(Perfluorohexyl)ethoxy]-1,2-epoxypropane
CAS Number: 122193-68-4
Molecular Formula: C11H9F13O2
Molecular Weight: 420.16720159999966
MDL Number: MFCD00143020
SMILES: FC(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(CCOCC1OC1)F

 

Upstream Synthesis Route
  • The compound 3-[2-(Perfluorohexyl)ethoxy]-1,2-epoxypropane is a valuable reagent in chemical synthesis, particularly in organic reactions where the unique properties of the perfluorohexyl group can be leveraged. This compound serves as an excellent building block for the synthesis of fluorinated organic compounds, which are of growing interest in various industries such as pharmaceuticals, materials science, and agrochemicals.One important application of this compound is in the modification of polymers and surfaces to impart specific properties such as increased hydrophobicity, chemical resistance, and thermal stability. The perfluorohexyl group provides a high degree of fluorination, leading to enhanced durability and performance of the resulting materials.Additionally, 3-[2-(Perfluorohexyl)ethoxy]-1,2-epoxypropane can be utilized in the synthesis of specialty chemicals and pharmaceutical intermediates due to its ability to introduce fluorine atoms into organic molecules. The presence of fluorine in these compounds often leads to improved pharmacokinetic properties, making them valuable candidates for drug development and other high-value applications.In summary, the compound 3-[2-(Perfluorohexyl)ethoxy]-1,2-epoxypropane plays a crucial role in chemical synthesis by enabling the efficient incorporation of fluorinated moieties into various organic compounds, thus expanding the scope of functional materials and fine chemicals that can be synthesized.
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