Produktname:11H-Benzofuro[3,2-b]carbazole

IUPAC Name:10-oxa-20-azapentacyclo[11.7.0.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]icosa-1,3(11),4(9),5,7,12,14(19),15,17-nonaene

CAS:1199350-22-5
Molekulare Formel:C18H11NO
Reinheit:95%+
Katalognummer:CM583500
Molekulargewicht:257.29

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Produkt-Details

CAS-Nr.:1199350-22-5
Molekulare Formel:C18H11NO
Schmelzpunkt:-
SMILES-Code:N1C2=CC3=C(OC4=C3C=CC=C4)C=C2C2=C1C=CC=C2
Dichte:
Katalognummer:CM583500
Molekulargewicht:257.29
Siedepunkt:
Mdl-Nr.:MFCD28154723
Lagerung:

Category Infos

Carbazoles
Carbazoles are an important class of nitrogen-containing heterocycles with a planar tricyclic skeleton consisting of two benzene rings fused on both sides of the central pyrrole ring, with a large aromatic system and a central nitrogen atom, showing broad of electron delocalization. The structure of this compound is based on the indole structure, but in which a second benzene ring is fused to a five-membered ring at positions 2-3 of the indole. Carbazole structural motifs are widely found in, but not limited to, a large number of natural alkaloids of plant or bacterial origin. Since many of these alkaloids are medically useful, exhibit a fairly wide range of biological activities (anticancer, anti-HIV, antibacterial, anti-Alzheimer's disease, anticoagulant, analgesic, antiepileptic, antidiabetic, antioxidant, etc.). Medicinal chemistry also uses carbazole motifs in synthetic drugs to combat hypertension, heart disease, and hepatitis C virus replication.
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Dibenzofurans
Dibenzofuran is an organic compound (C12H8O) consisting of two benzene rings fused to a central furan ring. Dibenzofuran can be synthesized by annealing and oxidative coupling methods of diphenyl ether, biphenyl derivatives, benzofuran, quinone. Most of the dibenzofuran-related natural products are metabolites of lichens or higher fungi. Lichen dibenzofurans appear to be formed by carbon-carbon oxidative coupling of orsellinic acid and its homologs.

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