Tribromoisocyanuric acid
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| Names | |
|---|---|
| Preferred IUPAC name 1,3,5-Tribromo-1,3,5-triazinane-2,4,6-trione | |
| Other names TBCA 1,3,5-tribromo-1,3,5-triazine | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| C3Br3N3O3 | |
| Molar mass | 366 g/mol |
| Appearance | colourless solid |
| Boiling point | decomposes |
| Solubility in sulfuric acid | Soluble |
| Structure | |
| planar | |
| 0 D | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards | lung irritant |
| Flash point | N/A |
| Related compounds | |
Related compounds | Cyanuric bromide Dibromoisocyanuric acid Trichloroisocyanuric acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Tribromoisocyanuric acid (C3Br3N3O3) is a chemical compound used as a reagent for bromination in organic synthesis.[1] It is a white crystalline powder with a strong bromine odour. It is similar to trichloroisocyanuric acid.
Uses
Tribromoisocyanuric acid is used for the bromination of aromatics and alkenes.
References
- ^ A New Regioselective Bromination of Activated Aromatic Rings, Almeida, L. S. de; Esteves, P. M.; Mattos, M. C. S. Synthesis 2006, No 2 , 221-223. DOI: 10.1055/s-2005-918511 (https://www.thieme-connect.com/products/ejournals/html/10.1055/s-2005-918511)
