Iodotrifluoroethylene
Iodotrifluoroethylene is a chemical compound with the formula C
2F
3I, belonging to the group of haloalkenes. It is a volatile colorless liquid. It is prepared by iodination of trifluorovinyl lithium.[1]
Names | |
---|---|
Preferred IUPAC name
1,1,2-Trifluoro-2-iodoethene | |
Other names
1,1,2-Trifluoro-2-iodoethylene, trifluoroiodoethylene, iodotrifluoroethylene | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.006.028 |
EC Number |
|
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C2F3I | |
Molar mass | 207.92 g/mol |
Density | 2.284 g/cm3 |
Boiling point | 30 °C (86 °F; 303 K) |
Hazards | |
Main hazards | Irritant (Xi) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
It can be used to synthesize trifluoronitrosoethylene by its reaction with nitric oxide under UV light, producing iodine as a byproduct:[2]
- 2 C
2F
3I + 2 NO → 2 C
2F
3NO + I
2
References
- Burdon, James; Coe, Paul L.; Haslock, Iain B.; Powell, Richard L. (1996). "The hydrofluorocarbon 1,1,1,2-tetrafluoroethane (HFC-134a) as a ready source of trifluorovinyllithium". Chemical Communications: 49. doi:10.1039/CC9960000049.
- Griffin, C. E.; Haszeldine, R. N . (1960). "Perfluoroalkyl derivatives of nitrogen. Part VIII. Trifluoronitrosoethylene and its polymers". Journal of the Chemical Society (Resumed): 1398–1406. doi:10.1039/JR9600001398.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.