19190-61-5

Usage

Uses

Used in Solvent Applications:
Butanoic acid, 2,2,3,3,4,4-hexafluoro-4-[(trifluoroethenyl)oxy]-, methyl ester is used as a solvent in various chemical processes due to its ability to dissolve a wide range of substances and its low toxicity.
Used as an Intermediate in Chemical Synthesis:
Butanoic acid, 2,2,3,3,4,4-hexafluoro-4-[(trifluoroethenyl)oxy]-, methyl
ester serves as an intermediate in the synthesis of other organic compounds, including pharmaceuticals and agrochemicals, due to its unique structure and reactivity.
Used in Pharmaceutical Production:
Butanoic acid, 2,2,3,3,4,4-hexafluoro-4-[(trifluoroethenyl)oxy]-, methyl ester is utilized in the production of pharmaceuticals, where its specific properties can contribute to the development of new drugs and medications.
Used in Agrochemical Production:
It is also employed in the creation of agrochemicals, where its unique chemical structure can be harnessed to develop more effective and targeted products for agricultural use.
Used in Organic Synthesis:
Butanoic acid, 2,2,3,3,4,4-hexafluoro-4-[(trifluoroethenyl)oxy]-, methyl
ester has potential applications in the field of organic synthesis, where its fluorinated and trifluoroethenyloxy groups can be exploited to create novel and useful molecules.
Used in Materials Science:
Butanoic acid, 2,2,3,3,4,4-hexafluoro-4-[(trifluoroethenyl)oxy]-, methyl ester is utilized in materials science for the development of new materials with specific properties, such as improved stability or reactivity.

Upstream product

• 67-56-1 methanol 
• 23276-05-3 Perfluoro-5-oxa-6-heptenoic acid fluoride 
• 64725-41-3 6-carbomethoxy-perfluoro-2-methyl-3-oxa-hexanoyl fluoride 
• 19190-57-9 perfluoro-2-methyl-3-oxaheptanedioyl fluoride 
• 55678-21-2 dimethyl perfluoro(2-methyl-3-oxa-heptane-1,7-dioate) 
• 63425-24-1 Methyl tetrafluoro-3-fluoroformylpropanate 

Downstream Products

• 67-56-1 methanol 
• 377-38-8 tetrafluorosuccinic acid 
• 356-36-5 dimethyl tetrafluorosuccinate 
• 73727-54-5 perfluoro-5-oxa-6-heptenoic acid 
• 69531-48-2 sodium 5-oxaperfluoro-6-heptenoate 
• 86556-80-1 4-(1,2-Dichloro-1,2,2-trifluoro-ethoxy)-2,2,3,3,4,4-hexafluoro-butyric acid methyl ester 
• 86556-81-2 perfluoro(4-vinyloxybutyric acid) chloride 
• 86556-82-3 C₉H₁₀Cl₂F₉O₃P 
• 120145-81-5 5,6-dichloro-4-oxa-2,2,3,3,5,6,6-heptafluorohexanoic acid 
• 79683-40-2 1,2-dichloro-6-iodo-1,1,2,4,4,5,5,6,6-nonafluoro-3-oxahexane 
• 143571-13-5 sodium 5,8-dioxa-6,9,9,9-tetrahydrononafluorononanoate 
• 143571-12-4 disodium 5-oxa-6-hydroheptafluoropimelate 
• 19190-59-1 Perfluor-5-oxa-6-heptensaeureamid 

Relevant academic research and scientific papers

Synthesis of perfluorinated vinyl ethers having ester group

A new efficient and convenient synthetic process of perfluorinated vinyl ethers containing an ester group was developed by pyrolysis in the presence of α-trifluoromethyl moiety without loss of -COF functional group followed by alcoholysis in high yield.

PROCESS FOR PRODUCING FLUORINATED COMPOUND

To provide a process for producing a desired perfluorinated product at a high yield in a fluorination reaction of a partially fluorinated ester. A perfluorinated compound (4) is obtained by fluorinating in a liquid phase a compound (3) (wherein the fluorine content is at least 30 mass %) obtained by reacting a compound (1) and a compound (2), wherein the compound (1) is HOCH2—RA—CH2OH, the compound (2) is X1C(═O)—C(RB)(RC)(RD), RA is a bivalent saturated hydrocarbon group or the like which has no hetero atom such as an etheric oxygen atom, X1 is a halogen atom, and —C(RB)(RC)(RD) is a branched group.

Method for producing fluorinated compound

Provided is a method for producing a desired perfluorinated product with high yield by a fluorination reaction of a partially fluorinated ester. A compound (3), which is produced by reacting a compound (1) with a compound (2) (and which has a fluorine content of 30 mass% or more), is fluorinated in a liquid phase to produce a perfluorinated compound (4), wherein the compound (1) is represented by the formula HOCH2-RA-CH2OH and the compound (2) is represented by the formula X1C(=O)-C(RB)(RC)(RD). RA represents a bivalent saturated hydrocarbon group or the like and does not have a hetero atom such as an ethereal oxygen atom. X1 represents a halogen atom, and -C(RB)(RC)(RD) represents a branched group.

Cyclization processes in pyrolysis of perfluorooxaalkanedicarboxylic acid derivatives

Formation of cyclic structures under the conditions of pyrolytic decarboxylation of perfluorooxaalkanedicarboxylic acids was studied.

Polyfluorinated ethers: IV.* By-products in the synthesis of polyfluorinated alkyl vinyl ethers in a solvating solvent

By-products formed in the synthesis of perfluoro(propyl vinyl ether), perfluoro(2-propoxypropyl vinyl ether), and methyl perfluoro(4-vinyloxybutanoate) in a solvating solvent have been studied. 1998 MAHK "Hayka/Interperiodica".

Use of Perfluoroalkylfluorosulfonates for Synthesizing Organofluorine Compounds

The possibility of using fluorosulfation for synthesizing perfluorovinyl and perfluorodivinyl ethers, and also perfluorocarboxylic and perfluorodicarboxylic acids, has been studied.