Nombre del producto:2-methylquinolin-8-yl 6-nitro-2-oxo-2H-chromene-3-carboxylate

IUPAC Name:2-methylquinolin-8-yl 6-nitro-2-oxo-2H-chromene-3-carboxylate

CAS:887198-04-1
Fórmula molecular:C20H12N2O6
Pureza:95%+
Número de catálogo:CM848030
Peso molecular:376.32

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Detalles del producto

Núm. De CAS :887198-04-1
Fórmula molecular:C20H12N2O6
Punto de fusión:-
Código de sonrisas:CC1=CC=C2C=CC=C(OC(=O)C3=CC4=CC(=CC=C4OC3=O)[N+]([O-])=O)C2=N1
Densidad:
Número de catálogo:CM848030
Peso molecular:376.32
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Quinolines
Quinolines are an important class of biologically active heterocyclic compounds, and their derivatives usually exhibit a variety of biological activities. They can be used as antimalarial drugs and in the preparation of other antimalarial drugs. Other important activities of quinoline derivatives include inhibitory activity against EGFR-TK and antipsychotic activity. Futhermore, quinoline scaffolds are present in various drug molecules, including the antimalarial drugs aablaquine, chloroquine, mefloquine and primaquine, and the antibacterial agents gatifloxacin, levofloxacin, and moxifloxacin.
Quinoline Price
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Coumarins
Coumarin occurs naturally in a variety of plants, such as lentils, sweet sawdust, vanilla grass, and sweet grass. Coumarin has a simple structure, benzopyrone, associated with different reaction centers. Coumarins are further subdivided into different classes: simple coumarins, pyranocoumarins, furanocoumarins, dicoumarins and isocoumarins. Coumarin derivatives are an important class of natural plant metabolites with various biological activities. They can also be synthesized artificially, and various synthetic coumarin derivatives (azoles, sulfonyls, furans, pyrazoles, etc.) have shown good anticancer, antitumor and antiproliferative activities. Coumarin derivatives are not only effective anticancer agents, but also possess minimum side effects. Based on different substitution patterns, these potential active substances show a great ability to modulate potential anticancer activities.

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