Nom du produit:quinolin-8-yl 6-methoxy-2-oxo-2H-chromene-3-carboxylate
IUPAC Name:quinolin-8-yl 6-methoxy-2-oxo-2H-chromene-3-carboxylate
- CAS：838904-25-9
- Formule moléculaire：C20H13NO5
- Pureté：95%+
- Numéro de catalogue：CM1012852
- Poids moléculaire：347.33
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Détails du produit
- N° CAS:838904-25-9
- Formule moléculaire:C20H13NO5
- Point de fusion:-
- Code SMILES:COC1=CC=C2OC(=O)C(=CC2=C1)C(=O)OC1=CC=CC2=CC=CN=C12
- Densité:
- Numéro de catalogue:CM1012852
- Poids moléculaire:347.33
- Point d'ébullition:
- N° Mdl:
- Stockage:
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
- if you have any question on quinoline price, we will give the professional answers to your short questions.
- 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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