3-chlorocarbazole Chemical Properties

InChI

InChI=1S/C12H8ClN/c13-8-5-6-12-10(7-8)9-3-1-2-4-11(9)14-12/h1-7,14H

InChIKey

CABSFELLEWZIAK-UHFFFAOYSA-N

SMILES

N1C2=C(C=CC=C2)C2=C1C=CC(Cl)=C2

3-chlorocarbazole Usage And Synthesis

Uses

3-Chloro-9H-carbazole is a standard for environmental testing and research. An aryl hydrocarbon receptor agonist. Substance for the characterization and biological potency of mono- to tetra-halogenated carbazoles.

References

[1] X. Kang. “Removal of 3-chlorocarbazole using a Fe/Ni bimetallic nanocomposite as an effective catalyst: characteristics and mechanism.” International Journal of Environmental Science and Technology 20 1 (2022): 859–870.
[2] Zhuyu Sun . “Degradation of 3-chlorocarbazole in water by sulfidated zero-valent iron/peroxymonosulfate system: Kinetics, influential factors, degradation products and pathways.” Chemosphere 296 (2022): Article 134016.
[3] Sergio M. Bonesi, Rosa Erra-Balsells. “On the synthesis and isolation of chlorocarbazoles obtained by chlorination of carbazoles.” Journal of Heterocyclic Chemistry 34 3 (2009): 877–889.

3-chlorocarbazole(2732-25-4)Related Product Information

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