- N-Vinylcarbazole
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N-vinylcarbazole[1] 9H-carbazoleOther names9-vinyl-9H-carbazole, NVCIdentifiers CAS number 1484-13-5 PubChem 15143 ChemSpider 14414 EC number 216-055-0 RTECS number FE6350000 Jmol-3D images Image 1 - c1cccc3c1c2c(cccc2)n3C=C
- InChI=InChI=1S/C14H11N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h2-10H,1H2
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, 100 kPa)Infobox references N-Vinylcarbazole is an organic compound used as a monomer in the production of poly(vinylcarbazole), a photoconductive polymer 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. p. 3–518. ISBN 978-0849304880.
- ^ a b Sigma-Aldrich 9-Vinylcarbazole product page
- ^ G. Burton, J. Holman, J. Lazonby, G. Pilling, D. Waddington (2000). Chemical Storylines (2nd ed.). 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.
Categories:- Carbazoles
- Monomers
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