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Usage

Uses

Used in the Production of Fluoropolymers:
PERFLUOROHEPT-2-ENE is used as a building block for the synthesis of fluoropolymers. These polymers are valued for their exceptional durability and resistance to harsh conditions, making them suitable for a wide range of industrial applications.
Used in the Chemical Industry:
In the chemical industry, PERFLUOROHEPT-2-ENE is utilized as a processing aid. Its properties allow it to improve the manufacturing process of various materials, enhancing their performance and quality.
Used in the Textile Industry:
PERFLUOROHEPT-2-ENE is used as a processing aid in the textile industry. It helps in producing textiles with enhanced properties, such as increased resistance to stains, water, and wear, making them more durable and long-lasting.
Used in the Food Packaging Industry:
In the food packaging sector, PERFLUOROHEPT-2-ENE is employed as a processing aid. Its use contributes to the creation of packaging materials with improved barrier properties, ensuring the freshness and safety of the packaged food products.

InChI:InChI=1/C7F14/c8-1(2(9)4(12,13)14)3(10,11)5(15,16)6(17,18)7(19,20)21/b2-1-

Upstream product

• 355-63-5 perfluoro-1-heptene 
• 755-25-9 perfluoro-1-hexene 
• 131393-38-9 perfluoro(n-butylcyclopropane) 

Relevant academic research and scientific papers

Electrophilic reactions of fluorocarbons under the action of aluminum chlorofluoride, a potent Lewis acid

A new Lewis acid - aluminum chlorofluoride - was demonstrated to be an effective catalyst for the isomerisation of fluoroolefins, polyfluorinated epoxides and cyclopropanes.At ambient temperature this catalyst converts perfluorobutadiene-1,3 into perfluorobutyne-2 and perfluoro(4-methylpentene-2) into perfluoro(2-methylpentene-2) in nearly quantitative yield.At 100 deg C, aluminum chlorofluoride causes the cleavage of perfluorinated tertiary amines. - Keywords: Electrophilic reactions; Fluorocarbons; Aluminum chlorofluoride; Lewis acid; NMR spectroscopy

ELECTROPHILIC ISOMERIZATION OF SUBSTITUTED PERFLUOROCYCLOPROPANES UNDER THE EFFECT OF SbF5

Perfluoro(alkoxycyclopropanes) are isomerized on heating in the presence of SbF5 into perfluoro(2-alkoxypropylenes), while perfluoro(alkylcyclopropanes) are isomerized into the corresponding internal fluoroolefins under the effect of SbF5.

Fluorosulfonation. Insertion of Sulfur Trioxide into Allylic C-F Bonds

Insertion of sulfur trioxide into allylic C-F bonds of both terminal and internal fluoro olefins is shown to form the most stable olefinic products.A mechanism involving fluoroallyl cations as intermediates is proposed.State-of-the-art ab initio calculations of the ground-state energies for two isomeric unsaturated fluoro ethers establish the slightly greater stability (5.7 kcal/mol) of a vinyl ether over the corresponding fluoro olefin.A description of the optimized geometries of these molecules is also presented.