Produktname:4-(Oxiran-2-ylmethoxy)-9H-carbazole

IUPAC Name:4-[(oxiran-2-yl)methoxy]-9H-carbazole

CAS:51997-51-4
Molekulare Formel:C15H13NO2
Reinheit:98%
Katalognummer:CM338676
Molekulargewicht:239.27

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Produkt-Details

CAS-Nr.:51997-51-4
Molekulare Formel:C15H13NO2
Schmelzpunkt:-
SMILES-Code:C1(NC2=C3C=CC=C2)=C3C(OCC4OC4)=CC=C1
Dichte:
Katalognummer:CM338676
Molekulargewicht:239.27
Siedepunkt:
Mdl-Nr.:MFCD03411884
Lagerung:

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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Oxiranes
Oxirane is a three-membered ring compound consisting of one oxygen atom and two carbon atoms. Oxirane is present in natural products such as cryptocin, which has anticancer properties, and azidomycin, trienone, and epoxidomycin, which have shown activity against drug-resistant leukemias and AIDS-related lymphomas. Other oxirane containing bioactive molecules have anti-inflammatory, immunosuppressive, and antitumor activities. Oxiranes are a strained ring susceptible to various nucleophilic, ring-opening or rearrangement reactions, so they are considered to be one of the most important intermediates in organic synthesis.

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