Produktname:Pyrazolo[4,3-a]carbazole,3,10-dihydro-3-phenyl-

IUPAC Name:3-phenyl-2H,3H-pyrazolo[4,3-a]carbazole

CAS:1613406-18-0
Molekulare Formel:C19H13N3
Reinheit:95%+
Katalognummer:CM573207
Molekulargewicht:283.33

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Produkt-Details

CAS-Nr.:1613406-18-0
Molekulare Formel:C19H13N3
Schmelzpunkt:-
SMILES-Code:N1C=C2C(=CC=C3C4=CC=CC=C4N=C23)N1C1=CC=CC=C1
Dichte:
Katalognummer:CM573207
Molekulargewicht:283.33
Siedepunkt:
Mdl-Nr.:
Lagerung:

Category Infos

Indazoles
Indazoles are a class of organic heterocyclic compounds, also known as 1,2-diazaindene and benzopyrazole. Indazole is a good bioisomer of phenol, which is more lipophilic than phenol and less prone to phase I and II metabolism. Indazole derivatives have a wide range of biological activities, and it has been confirmed that indazole compounds have anti-tumor, analgesic, anti-inflammatory and other drug activities. Anticancer is the most important application field of indazole drugs. Renal cell carcinoma, solid tumor, nausea and vomiting caused by chemotherapy and leukemia are the main indications of this structural backbone drug.
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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