cas 1922121-95-6|| where to buy 9H-Carbazole,2-(4-dibenzofuranyl)-

Product Name: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; Molecular Formula：C24H15NO; Purity：95%+

: Catalog Number：CM573201; Molecular Weight：333.39

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CM573201-100mg	in stock	ƀƻƙ
CM573201-250mg	in stock	ȁǕƱ
CM573201-1g	in stock	ƱȬȁ

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Product Details

: CAS NO:1922121-95-6; Molecular Formula:C24H15NO; Melting Point:-; Smiles Code:N1C2=CC(=CC=C2C2=C1C=CC=C2)C1=CC=CC2=C1OC1=C2C=CC=C1; Density:

: Catalog Number:CM573201; Molecular Weight:333.39; Boiling Point:; MDL No:; Storage:

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.

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