62361-02-8

Basic information

• Product Name: methyl 2,2,3,3,4,4-hexafluoro-4-[1,2,2-trifluoro-2-[(trifluorovinyl)oxy]-1-(trifluoromethyl)ethoxy]butyrate
• Synonyms: methyl 2,2,3,3,4,4-hexafluoro-4-[1,2,2-trifluoro-2-[(trifluorovinyl)oxy]-1-(trifluoromethyl)ethoxy]butyrate;2,2,3,3,4,4-Hexafluoro-4-[1-(trifluoromethyl)-1,2,2-trifluoro-2-[(trifluoroethenyl)oxy]ethoxy]butyric acid methyl ester;2,2,3,3,4,4-Hexafluoro-4-[1,2,2-trifluoro-2-[(trifluoroethenyl)oxy]-1-(trifluoromethyl)ethoxy]butanoic acid methyl ester
• CAS NO: 62361-02-8
• Molecular Formula: C₁₀H₃F₁₅O₄
• Molecular Weight: 472.104468
• EINECS: 263-524-0
• Mol File: 62361-02-8.mol

Chemical Properties

• Boiling Point: 260.5°Cat760mmHg
• Flash Point: 108.1°C
• Appearance: /
• Density: 1.656g/cm³
• Vapor Pressure: 0.0122mmHg at 25°C
• Refractive Index: 1.314
• CAS DataBase Reference: methyl 2,2,3,3,4,4-hexafluoro-4-[1,2,2-trifluoro-2-[(trifluorovinyl)oxy]-1-(trifluoromethyl)ethoxy]butyrate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,2,3,3,4,4-hexafluoro-4-[1,2,2-trifluoro-2-[(trifluorovinyl)oxy]-1-(trifluoromethyl)ethoxy]butyrate(62361-02-8)
• EPA Substance Registry System: methyl 2,2,3,3,4,4-hexafluoro-4-[1,2,2-trifluoro-2-[(trifluorovinyl)oxy]-1-(trifluoromethyl)ethoxy]butyrate(62361-02-8)

Safety Data

• Hazardous Substances Data: 62361-02-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H3F15O4/c1-27-4(26)5(14,15)6(16,17)9(22,23)29-7(18,8(19,20)21)10(24,25)28-3(13)2(11)12/h1H3

Upstream product

• 67-56-1 methanol 
• 69905-79-9 2,2,3,3,4,4-hexafluoro-4-[1,2,2-trifluoro-2-(1,2,2,2-tetrafluoro-1-fluorocarbonyl-ethoxy)-1-trifluoromethyl-ethoxy]-butyryl fluoride 

Relevant articles and documents

Process for producing fluorinated vinyl ether

There is provided a process for producing a fluorinated vinyl ether from a fluorinated acid fluoride compound having an ester group as a precursor of a carboxylic acid group, or a SO2F group as a precursor of a sulfonic acid group, in high yield by simple operations. Said process is a production process comprising pyrolyzing a carboxylic acid potassium salt with a specific structure represented by the following formula in the absence of a solvent and/or while maintaining the salt in the solid state: wherein X is —CO2R or —SO2F, and R is an alkyl group.

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.