cas 913737-84-5|| where to buy 2,8-Bis(9-carbazolyl)dibenzofuran

Nom du produit:2,8-Bis(9-carbazolyl)dibenzofuran

IUPAC Name:9-[12-(9H-carbazol-9-yl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-4-yl]-9H-carbazole

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: N° CAS:913737-84-5; Formule moléculaire:C36H22N2O; Point de fusion:-; Code SMILES:O1C2=C(C=C(C=C2)N2C3=C(C=CC=C3)C3=C2C=CC=C3)C2=C1C=CC(=C2)N1C2=C(C=CC=C2)C2=C1C=CC=C2; Densité:

: Numéro de catalogue:CM621546; Poids moléculaire:498.59; Point d'ébullition:; N° Mdl:; Stockage:

: 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.