N-Vinylcarbazole
From Wikipedia, the free encyclopedia
| N-vinylcarbazole[1] | |
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| IUPAC name 9-ethenyl-9H-carbazole | |
| Other names 9-vinyl-9H-carbazole, NVC | |
| Identifiers | |
| CAS number | 1484-13-5  |
| PubChem | 15143 |
| ChemSpider | 14414  |
| EC number | 216-055-0 |
| RTECS number | FE6350000 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C14H11N |
| Molar mass | 193.244 g mol−1 |
| Appearance | pale brown crystalline solid[2] |
| Melting point | 66 °C |
| Boiling point | 154-155 °C, 3 mmHg[2] |
| Solubility in water | insoluble |
| Solubility in diethyl ether | very soluble |
| (verify) (what is: /?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
N-Vinylcarbazole is an organic compound used as a monomer in the production of poly(vinylcarbazole), a conductive polymer, in which conductivity is photon dependend. The compound is used in the photoreceptors of photocopiers.[3] Upon exposure to γ-irradiation, N-vinylcarbazole undergoes solid-state polymerisation.[4]
Related compounds
References
- ↑ Lide, David R. (2008). CRC Handbook of Chemistry and Physics, 89th Edition. CRC Press. pp. 3–518. ISBN 978-0-8493-0488-0.
- ↑ 2.0 2.1 Sigma-Aldrich 9-Vinylcarbazole product page
- ↑ G. Burton, J. Holman, J. Lazonby, G. Pilling, D. Waddington (2000). Chemical Storylines (2nd ed.). Heinemann Educational Publishers. pp. 121–122. ISBN 0-435-63119-5.
- ↑ K. Tsutsui, K. Hirotsu, M. Umesaki, M. Kurahashi, A. Shimada, T. Higuchi (1976). "Structural chemistry of polymerizable monomers. I. Crystal structure of N-vinylcarbazole". Acta Cryst. B32: 3049–3053. doi:10.1107/S0567740876009527.
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