cas 1246308-85-9|| where to buy 12H-Benzofuro[3,2-a]carbazole

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

IUPAC Name:9-oxa-20-azapentacyclo[11.7.0.0²,¹⁰.0³,⁸.0¹⁴,¹⁹]icosa-1(13),2(10),3(8),4,6,11,14(19),15,17-nonaene

: CAS：1246308-85-9; Molecular Formula：C18H11NO; Purity：95%+

: Catalog Number：CM616240; Molecular Weight：257.29

Packing Unit	Available Stock	Price($)
CM616240-5g	in stock	ȬƙŴ
CM616240-25g	in stock	ǧțǧ

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Product Details

: CAS NO:1246308-85-9; Molecular Formula:C18H11NO; Melting Point:-; Smiles Code:N1C2=C(C=CC=C2)C2=C1C1=C(OC3=C1C=CC=C3)C=C2; Density:

: Catalog Number:CM616240; Molecular Weight:257.29; 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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