N-Vinylcarbazole

N-vinylcarbazole^[1]
Names
	Preferred IUPAC name 9-Ethenyl-9H-carbazole
	Other names 9-Vinyl-9H-carbazole, NVC
Identifiers
CAS Number	1484-13-5 ;
3D model (JSmol)	Interactive image;
ChemSpider	14414 ;
ECHA InfoCard	100.014.596
EC Number	216-055-0;
PubChem CID	15143;
RTECS number	FE6350000;
UNII	D629AMY6F9 ;
CompTox Dashboard (EPA)	DTXSID4022155 ;
	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 Key: KKFHAJHLJHVUDM-UHFFFAOYSA-N;
	SMILES c1cccc3c1c2c(cccc2)n3C=C;
Properties
Chemical formula	C14H11N
Molar mass	193.244 g⋅mol−1
Appearance	Pale brown crystalline solid
Melting point	66 °C (151 °F; 339 K)
Boiling point	154 to 155 °C (309 to 311 °F; 427 to 428 K) 3 mmHg
Solubility in water	Insoluble
Solubility in diethyl ether	Very soluble
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

N-Vinylcarbazole is an organic compound used as a monomer in the production of poly(vinylcarbazole),^[3] a conductive polymer, in which conductivity is photon-dependent. The benzine compound is used in the photoreceptors of photocopiers.^[4] Upon exposure to γ-irradiation, N-vinylcarbazole undergoes solid-state polymerisation.^[5]

It is produced by the vinylation of carbazole with acetylene in the presence of base.^[6]

Related compounds

^ Lide, David R. (2008). CRC Handbook of Chemistry and Physics, 89th Edition. CRC Press. pp. 3–518. ISBN 978-0-8493-0488-0.
^ ^a ^b Sigma-Aldrich 9-Vinylcarbazole product page
^ Conti, Francsco (June 2006). "Nuova via di sintesi del vinilcarbazolo". La Chimica & L'Industria (in Italian) (5). Società Chimica Italiana: 82.
^ 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 Crystallogr. B. 32: 3049–3053. doi:10.1107/S0567740876009527.
^ Pässler, Peter; Hefner, Werner; Buckl, Klaus; Meinass, Helmut; Meiswinkel, Andreas; Wernicke, Hans-Jürgen; Ebersberg, Günter; Müller, Richard; Bässler, Jürgen; Behringer, Hartmut; Mayer, Dieter (2008). "Acetylene Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a01_097.pub3. ISBN 3527306730.