Produktname:7-methoxy-3-[5-(pyrazin-2-yl)-1,3,4-oxadiazol-2-yl]-2H-chromen-2-one
IUPAC Name:7-methoxy-3-[5-(pyrazin-2-yl)-1,3,4-oxadiazol-2-yl]-2H-chromen-2-one
- CAS:2320725-14-0
- Molekulare Formel:C16H10N4O4
- Reinheit:95%+
- Katalognummer:CM910408
- Molekulargewicht:322.28
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Produkt-Details
- CAS-Nr.:2320725-14-0
- Molekulare Formel:C16H10N4O4
- Schmelzpunkt:-
- SMILES-Code:COC1=CC=C2C=C(C3=NN=C(O3)C3=CN=CC=N3)C(=O)OC2=C1
- Dichte:
- Katalognummer:CM910408
- Molekulargewicht:322.28
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
Category Infos
- Pyrazines
- Pyrazine is a heterocyclic aromatic organic compound with chemical formula C4H4N2. The marketed pyrazine drugs are mainly distributed in the field of anti-tumor and anti-infection. In recent years, there have been many new drugs in various fields, and there are some new target drugs worthy of attention.
- pyrazine,pyrazine price
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- Oxadiazoles
- Oxadiazoles are a class of heterocyclic aromatic compounds with the molecular formula C2H2N2O, which have special biological activities and thermodynamic properties. Five-membered heterocyclic moieties composed of three or two heteroatoms are of great interest to researchers because these compounds show significant therapeutic potential. These heterocycles can serve as a building block for the development of novel molecular structures.
- 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.