Название продукции:14H-Benzo[c]benzofuro[2,3-a]carbazole

IUPAC Name:3-oxa-24-azahexacyclo[15.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁶.0¹⁸,²³]tetracosa-1(17),2(10),4(9),5,7,11(16),12,14,18(23),19,21-undecaene

CAS:1678511-52-8
Молекулярная формула:C22H13NO
Чистота:95%+
Номер в каталоге:CM616239
Молекулярная масса:307.35

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Информация о продукции

Номер CAS:1678511-52-8
Молекулярная формула:C22H13NO
Точка плавления:-
Smiles-код:N1C2=C(C=CC=C2)C2=C1C1=C(C3=C(O1)C=CC=C3)C1=C2C=CC=C1
Плотность:
Номер в каталоге:CM616239
Молекулярная масса:307.35
Точка кипения:
Номер Mdl:
Хранение:

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.
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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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