cas 1338919-70-2|| where to buy 12H-Benzofuro[2,3-a]carbazole

Produktname:12H-Benzofuro[2,3-a]carbazole

IUPAC Name:3-oxa-20-azapentacyclo[11.7.0.0²,¹⁰.0⁴,⁹.0¹⁴,¹⁹]icosa-1(13),2(10),4,6,8,11,14(19),15,17-nonaene

: CAS：1338919-70-2; Molekulare Formel：C18H11NO; Reinheit：97%

: Katalognummer：CM338663; Molekulargewicht：257.29

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Produkt-Details

: CAS-Nr.:1338919-70-2; Molekulare Formel:C18H11NO; Schmelzpunkt:-; SMILES-Code:C1(NC2=C3C=CC=C2)=C3C=CC4=C1OC5=CC=CC=C54; Dichte:

: Katalognummer:CM338663; Molekulargewicht:257.29; Siedepunkt:; Mdl-Nr.:; Lagerung:2-8°C, protect from light

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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