31898-68-7

  • Product Name:2,2-Bis(Trifluoromethyl)Oxirane
  • MF:C4H2F6O
  • Purity:99%
  • Molecular Weight:180.05
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Product Details

Cost-effective and customizable 2,2-Bis(Trifluoromethyl)Oxirane 31898-68-7 for sale

  • Molecular Formula:C4H2F6O
  • Molecular Weight:180.05
  • Vapor Pressure:523.193mmHg at 25°C 
  • Refractive Index:1.291 
  • Boiling Point:60.36 °C at 760 mmHg 
  • Flash Point:-4.738 °C 
  • PSA:12.53000 
  • Density:1.654 g/cm3 
  • LogP:1.88000 

2,2-Bis(trifluoromethyl)oxirane(Cas 31898-68-7) Usage

Use Description

2,2-Bis(trifluoromethyl)oxirane, also known as bis(trifluoromethyl)ethylene oxide, has several important applications across various fields. In the field of organic synthesis, it serves as a versatile building block for the creation of complex organic molecules. Its trifluoromethyl groups can be selectively modified to introduce desired chemical functionalities, making it valuable for drug discovery and the synthesis of specialty chemicals. In the realm of materials science, 2,2-Bis(trifluoromethyl)oxirane can be used as a monomer in the preparation of specialty polymers and materials with unique properties, including high thermal stability and resistance to chemical degradation. Additionally, in the field of fluorine chemistry, it contributes to the development of novel fluorinated compounds with potential applications in pharmaceuticals, agrochemicals, and materials. Its multifaceted utility underscores its significance in advancing organic chemistry, materials science, and the discovery of new molecules with diverse applications.

InChI:InChI=1/C4H2F6O/c5-1-2(3(6,7)8)4(9,10)11-2/h1H2

31898-68-7 Relevant articles

New partially fluorinated epoxides by oxidation of olefins with sodium hypohalites under phase transfer catalysis

Petrov, Viacheslav A.,Marshall, Will J.,Krespan, Carl G.,Cherstkov, Victor F.,Avetisian, Era A.

, p. 99 - 105 (2004)

Partially fluorinated epoxides can be re...

Reactions of 2,2-bis(trifluoromethyl)oxirane with alcohols under phase transfer catalysis

Petrov, Viacheslav A.

, p. 531 - 536 (2004)

It was demonstrated that the reaction of...

Chiral fluorous dialkoxy-diamino zirconium complexes: Synthesis and use in stereospecific polymerization of 1-hexene

Kirillov, Evgueni,Lavanant, Laurent,Thomas, Christophe,Roisnel, Thierry,Chi, Yun,Carpentier, Jean-Francois

, p. 923 - 935 (2007)

New catalysts for the isospecific polyme...

Preparation and characterization of volatile alkaline-earth metal complexes with multiply coordinated aminoalkoxide ligands

Chi,Ranjan,Chou,Liu,Peng,Lee

, p. 2462 - 2466 (2001)

The aminoalkoxide complexes Sr(amak)2 (1...

PREPARATION OF 2,2-BIS (FLUOROALKYL) OXIRANE AND PREPARATION OF PHOTOACID GENERATOR THEREFROM

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Page/Page column 7, (2013/02/28)

A 2,2-bis(fluoroalkyl)oxirane (A) is pre...

PROCESS FOR PREPARING HEXAFLUOROISOBUTENE EPOXIDE

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Page/Page column 1-2, (2008/12/07)

Processes for preparing hexafluoroisobut...

POLYFLUORINATED EPOXIDES AND ASSOCIATED POLYMERS AND PROCESSES

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Page 3, (2008/06/13)

A method for producing partially fluorin...

31898-68-7 Process route

2-trifluoromethyl-3,3,3-trifluoropropene
382-10-5

2-trifluoromethyl-3,3,3-trifluoropropene

2,2-bis(trifluoromethyl)oxirane
31898-68-7

2,2-bis(trifluoromethyl)oxirane

Hexafluoroacetone
684-16-2

Hexafluoroacetone

Conditions
Conditions Yield
With oxygen; at 230 ℃; for 12h; under 10343.2 Torr; Product distribution / selectivity;
hexafluoroisobutylene
1027143-59-4

hexafluoroisobutylene

2,2-bis(trifluoromethyl)oxirane
31898-68-7

2,2-bis(trifluoromethyl)oxirane

Conditions
Conditions Yield
With sodium hypochlorite; Aliquat 336; at -5 - 2 ℃; for 1.5 - 2h;
86%

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