Tetrabromoethylene
Tetrabromoethylene is a brominated derivative of ethylene. Tetrabromoethylene is a potential fungicide and bactericide on fruits. It was used in mineral separation.
Names | |
---|---|
Preferred IUPAC name
Tetrabromoethene | |
Other names
Perbromoethene | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.001.084 |
EC Number |
|
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C2Br4 | |
Molar mass | 343.638 g·mol−1 |
Appearance | Colorless crystal |
Melting point | 50 °C (122 °F; 323 K) |
Boiling point | 226 °C (439 °F; 499 K) |
-114.8·10−6 cm3/mol | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
It is prepared from acetylene and bromine in multiple steps. One method involves dehydrobromination of pentabromoethane, other method involves bromination of dibromoethylene in chloroform. Reaction of mercuric acetylide and bromine also gives tetrabromoethylene. It can be produced by oxybrominating butane with free oxygen and bromine.
Tetrabromoethylene gives tribromoacetyl bromide upon treatment with fuming nitric acid.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.