41004-33-5

Usage

Uses

Used in Refrigeration Industry:
2-Butene, 1,1,1,2,4,4,4-heptafluoro-3-(trifluoromethyl)is used as a refrigerant for cooling systems in the refrigeration industry. Its non-flammable and non-toxic properties make it a safe and efficient alternative to traditional refrigerants.
Used in Foam Production:
2-Butene, 1,1,1,2,4,4,4-heptafluoro-3-(trifluoromethyl)is used as a blowing agent for the production of foams in various industries. Its ability to create stable foams with low environmental impact makes it a preferred choice for manufacturing insulation materials, packaging materials, and other foam-based products.
Used as an Environmentally Friendly Alternative:
2-Butene, 1,1,1,2,4,4,4-heptafluoro-3-(trifluoromethyl)is used as a substitute for harmful chlorofluorocarbons (CFCs) in various applications. Its low global warming potential and non-toxic nature make it a suitable and eco-friendly alternative for reducing the environmental impact of industrial processes.

Upstream product

• 21581-82-8 decafluoro-3-methyl-1-butene 
• 124-41-4 sodium methylate 
• 685-01-8 2-iodoperfluoro-3-methylbut-2-ene 
• 354-34-7 trifluoroacetyl fluoride 
• 1540-04-1 hexafluoroisopropylidenetriethoxyphosphorane 
• 120615-52-3 perfluoro-2,3,3,4-tetramethylpentane 
• 41004-27-7 2-Trifluoromethyl-1,1,1,2,3,4,4-heptafluoro-4-iodobutane 

Downstream Products

• 41004-40-4 2-Methoxynonafluoro-3-methylbutane 
• 41004-34-6 Dimethyl-(3,3,3-trifluoro-1,2-bis-trifluoromethyl-propenyl)-amine 
• 102780-80-3 tris(dimethylamino)sulfonium 1,1,1,3,3,4,4,4-octafluoro-2-(trifluoro-methyl)-2-butanide 
• 21581-82-8 decafluoro-3-methyl-1-butene 
• 71127-01-0 2-Methoxynonafluoro-3-methylbut-2-ene 
• 41004-42-6 2,3-dichloro-1,1,1,2,4,4,4-heptafluoro-3-trifluoromethyl-butane 
• 41004-41-5 1,1,1,2,4,4,4-heptafluoro-3-trifluoromethyl-butane 

Relevant academic research and scientific papers

Reactions of novel unsaturated fluorocarbons

Novel fluorinated mono-enes and di-enes have been synthesised via telomerisation reactions using (CF3)2CFI with CF2=CH2 and also with CF2=CFH. Cyclo-additions with diazomethane occur readily to give Δ1 or Δ2 pyrazolines, depending on the system, and nucleophilic attack occurs with methanol and with fluoride ion. In the latter case, stable carbanions have been observed. A novel free-radical route to seven-membered rings, arising from cyclo-addition of dimethyl- and diethyl-ethers to the diene [(CF3)2C=CHCF2-]2 (3), has been developed.

Thermal decomposition of branched-chain perfluoroalkanes

The pyrolysis of some branched perfluoroalkanes has been studied.Homolytic cleavage of the most hindered carbon-carbon bond occurs, followed by coupling and rearrangement of the radicals so formed.This mechanism accounts for all the reaction products.Some kinetic and thermodynamic data are presented.

Fluoro-olefin Chemistry. Part 13. A Further Route to Perfluoro-2,3-dimethylbut-2-ene and the Photochemical Rearrangement of Some Perfluoro-alkyl Olefins

Perfluoro-2,3-dimethylbut-2-ene is conveniently prepared from perfluoro-(2,2,4,4-tetramethyldithietan) at 325 deg C.Under u.v. irradiation it is efficiently isomerised to perfluoro-2,3-dimethylbut-1-ene.Perfluoro-2-methylbut-2-ene and perfluoro-3-methylpent-2-ene are also isomerised photochemically, but more slowly, migration of fluorine being exclusively to the RFCF: group.In the presence of fluoride ion the internal olefins are reformed quantitatively.