Nom du produit:9H-Carbazole,2-(4-dibenzofuranyl)-

IUPAC Name:2-{8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl}-9H-carbazole

CAS:1922121-95-6
Formule moléculaire:C24H15NO
Pureté:95%+
Numéro de catalogue:CM573201
Poids moléculaire:333.39

Unité d'emballage Stock disponible Prix($) Quantité
CM573201-100mg in stock ŵưƎ
CM573201-250mg in stock ǶNJƦ
CM573201-1g in stock ƦȡǶ

Pour une utilisation en R&D uniquement..

Formulaire de demande

   refresh    

Détails du produit

N° CAS:1922121-95-6
Formule moléculaire:C24H15NO
Point de fusion:-
Code SMILES:N1C2=CC(=CC=C2C2=C1C=CC=C2)C1=CC=CC2=C1OC1=C2C=CC=C1
Densité:
Numéro de catalogue:CM573201
Poids moléculaire:333.39
Point d'ébullition:
N° Mdl:
Stockage:

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.
carbazole price
Buy low price, high quality carbazole,choose our products, warmly welcome new and old customers to visit and patronize!
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.

Related Products