cas 2410401-58-8|| where to buy 9H-Carbazol-2-amine, N-3-dibenzofuranyl-9-phenyl-

Produktname:9H-Carbazol-2-amine, N-3-dibenzofuranyl-9-phenyl-

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

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CM637504-5g	in stock	ƿȺƎ

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: CAS-Nr.:2410401-58-8; Molekulare Formel:C30H20N2O; Schmelzpunkt:-; SMILES-Code:N(C1=CC2=C(C=C1)C1=C(O2)C=CC=C1)C1=CC=C2C(=C1)N(C1=C2C=CC=C1)C1=CC=CC=C1; Dichte:

: Katalognummer:CM637504; Molekulargewicht:424.5; Siedepunkt:; Mdl-Nr.:; Lagerung:

: 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.