161611-74-1

Basic information

• Product Name: 2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole
• Synonyms: 1,3-dioxole, 2,2,4-trifluoro-5-(trifluoromethoxy)-; 2,2,4-Trifluoro-5-(trifluoromethoxy)-1,3-dioxole
• CAS NO: 161611-74-1
• Molecular Formula: C₄F₆O₃
• Molecular Weight: 210.0314
• Mol File: 161611-74-1.mol

Chemical Properties

• Boiling Point: 36.645°C at 760 mmHg
• Flash Point: -19.348°C
• Density: 1.74g/cm³
• Vapor Pressure: 499.754mmHg at 25°C
• Refractive Index: 1.32
• CAS DataBase Reference: 2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole(161611-74-1)
• EPA Substance Registry System: 2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole(161611-74-1)

Safety Data

• Hazardous Substances Data: 161611-74-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Production:
2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole is utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its fluorinated nature and reactivity make it a valuable component in the development of new drugs and pesticides.
Used in Organic Synthesis as a Solvent:
In the field of organic synthesis, 2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole serves as a solvent, facilitating various chemical reactions. Its ability to dissolve a wide range of compounds and its stability under different reaction conditions contribute to its utility in this application.
Used in Chemical Research as a Reagent:
2,2,4-trifluoro-5-(trifluoromethoxy)-1,3-dioxole is employed as a reagent in chemical research, where its unique properties allow for the exploration of new chemical reactions and the synthesis of novel compounds.
Used in Polymer, Plastic, and Coating Manufacturing:
This fluorinated compound finds application in the manufacturing of polymers, plastics, and coatings, where its chemical structure imparts specific properties such as resistance to heat, chemicals, and UV radiation.

Upstream product

• 373-91-1 hypofluorous acid trifluoromethyl ester 

Relevant articles and documents

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Dehalogenation process

A process for obtaining vinyl compounds by dehalogenation of halofluorinated compounds having a linear, branched or cyclic structure, said halofluorinated compounds containing in the molecule at least one group: wherein Y1 and Y2, equal to or different from each other, are selected from Cl, Br, I; wherein the halofluorinated compounds are dehalogenated in the presence of a transition metal, or of transition metal couples, by operating in a biphasic system of solvents immiscible among each other, formed of a (per)fluorinated solvent and a dipolar aprotic or protic solvent (co-solvent), wherein the ratio moles co-solvent/equivalents of the halofluorinated compound ranges from 0.5 to 10, preferably from 0.5 to 5, still more preferably from 1 to 3.