31898-68-7
- Product Name:2,2-Bis(Trifluoromethyl)Oxirane
- MF:C4H2F6O
- Purity:99%
- Molecular Weight:180.05
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
-
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
-
-
382-10-5
2-trifluoromethyl-3,3,3-trifluoropropene
-
-
31898-68-7
2,2-bis(trifluoromethyl)oxirane
-
-
684-16-2
Hexafluoroacetone
| Conditions | Yield |
|---|---|
|
With
oxygen;
at 230 ℃;
for 12h;
under 10343.2 Torr;
Product distribution / selectivity;
|
-
-
1027143-59-4
hexafluoroisobutylene
-
-
31898-68-7
2,2-bis(trifluoromethyl)oxirane
| Conditions | Yield |
|---|---|
|
With
sodium hypochlorite;
Aliquat 336;
at -5 - 2 ℃;
for 1.5 - 2h;
|
86% |
31898-68-7 Upstream products
-
186581-53-3
diazomethane
-
684-16-2
Hexafluoroacetone
-
382-10-5
2-trifluoromethyl-3,3,3-trifluoropropene
-
1027143-59-4
hexafluoroisobutylene
31898-68-7 Downstream products
-
305851-51-8
2-benzyl-1,1,1,3,3,3-hexafluoro-2-propanol
-
54841-08-6
1,1,4,4-tetrakis(trifluoromethyl)butane-1,4-diol
-
503169-76-4
1,1-bis(trifluoromethyl)-2-bromoethanol
-
98331-76-1
2-[(diphenylphosphanyl)methyl]-1,1,1,3,3,3-hexafluoro-propan-2-ol
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