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Usage

Uses

Used in Chemical Synthesis:
Allyl 2,2,3,3-Tetrafluoropropyl Ether is used as a chemical intermediate for the synthesis of other compounds in various industries. Its reactive propyl ether group allows it to participate in a wide range of chemical reactions, making it a versatile component in the production of various products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Allyl 2,2,3,3-Tetrafluoropropyl Ether is used as a building block for the development of new drugs. Its unique fluoroether property can contribute to the creation of novel molecular structures with potential therapeutic applications.
Used in Material Science:
In material science, Allyl 2,2,3,3-Tetrafluoropropyl Ether is used as a component in the development of advanced materials with specific properties. Its incorporation into polymers and other materials can lead to the creation of new products with improved characteristics, such as enhanced durability or chemical resistance.
Used in Electronics Industry:
In the electronics industry, Allyl 2,2,3,3-Tetrafluoropropyl Ether is used as a component in the manufacturing of electronic devices and components. Its unique properties can contribute to the development of new materials with improved performance, such as increased heat resistance or reduced electrical conductivity.
Used in Automotive Industry:
In the automotive industry, Allyl 2,2,3,3-Tetrafluoropropyl Ether is used as a component in the production of various automotive parts and materials. Its incorporation into materials can lead to the development of new products with improved performance, such as increased durability or reduced weight.

Upstream product

• 76-37-9 2,2,3,3-tetrafluoropropanol 
• 107-05-1 3-chloroprop-1-ene 
• 19932-26-4 3-((2',2',3',3'-tetrafluoropropanoxy)methyl)oxirane 
• 1137575-85-9 2[(3,3,2,2-tetrafluoropropoxy)methyl]thiirane 
• 110920-07-5 3-[(chlorosulfinyl)oxy]-1,1,2,2-tetrafluoropropane 
• 107-18-6 allyl alcohol 

Relevant academic research and scientific papers

Features of the reaction of polyfluoroalkyl chlorolsulfites with allyl alcohol

Unlike the saturated aliphatic and aromatic alcohols, allyl alcohol under the same conditions reacts with polyfluoroalkyl chlorosulfites to form not ethers, but polyfluorinated alcohols. The exception is polyfluoroalkyl chlorosulfites with the chain length of more than five carbon atoms. Allyl ethers of polyfluorinated alcohols of general formula CH2=CHCH 2OCH2(CF2CF2)nH (n = 1-3) were obtained, when the reaction proceeded in the presence of potassium carbonate, owing to its participation in a specific orientation of the reaction centers in the resulting intermediate structure, which is easily transformed into allyl ethers of polyfluorinated alcohols. Pleiades Publishing, Ltd., 2011.

Oligosiloxane mit funktionellen Gruppen. XI. Zur Synthese von Siloxanyl- und Na-Sulfo-Propoxy-α,α,ω-trihydroperfluoralkanen

Several α,α,ω-trihydroperfluoroalkylallyl ethers (2a-c) have been prepared in excellent yields by phase transfer catalysis of α,α',ω-trihydroperfluoroalcoholes and allyl chloride using 3-siloxanylpropylammonium halides as a catalyst.In the presence of a Pt-olefin complex the hydrosilylation of 2a-c with H-siloxanes affords 3-siloxanylpropoxy-α,α',ω-trihydrofluoroalkanes in high yields.The reaction of 2a-c with aqueous NaHSO3/Na2SO3 solution gives anionic fluorosurfactants (4c) beginning with n = 3.

Thermal desulfurization of (Alkoxymethyl)thiiranes

Reaction of (alkoxymethyl)oxiranes with thiourea in methanol has afforded the corresponding thiiranes, and catalyst-free thermal desulfurization of the products has been studied. The major products of desulfurization are alcohols and alkenes, both in the cases of (polyfluoroalkyloxymethyl)thiiranes and their non-fluorinated analogs. Longer alkyl chain in thiiranes favors formation of alcohols over alkenes formation in the course of desulfurization.