Tribromoethylene
| Names | |
|---|---|
| IUPAC name
tribromoethene | |
| Other names
ethylene tribromide | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.009.020 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C2HBr3 | |
| Molar mass | 264.742 g·mol−1 |
| Density | 2.5415 g/cm³ |
| Melting point | −52 °C (−62 °F; 221 K) |
| Boiling point | 164 °C (327 °F; 437 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H302, H312, H315, H319, H332, H335 | |
| P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Tribromoethylene is a bromoalkene and a trihaloethylene with the chemical formula C2HBr3. It can be made from 1,1,2,2-tetrabromoethane.
Tribromoethylene reacts with potassium hydroxide to yield dibromoacetylene via dehydrobromination, this reaction is analogous to the synthesis of dichloroacetylene from trichloroethylene. Tribromoethylene reacts with nitric acid to form dibromoacetic acid.