Nom du produit:N-[2-(5,8-dimethoxy-2-oxo-1,2-dihydroquinolin-3-yl)ethyl]-1-benzofuran-2-carboxamide
IUPAC Name:N-[2-(5,8-dimethoxy-2-oxo-1,2-dihydroquinolin-3-yl)ethyl]-1-benzofuran-2-carboxamide
- CAS:851404-32-5
- Formule moléculaire:C22H20N2O5
- Pureté:95%+
- Numéro de catalogue:CM986314
- Poids moléculaire:392.41
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Détails du produit
- N° CAS:851404-32-5
- Formule moléculaire:C22H20N2O5
- Point de fusion:-
- Code SMILES:COC1=C2NC(=O)C(CCNC(=O)C3=CC4=CC=CC=C4O3)=CC2=C(OC)C=C1
- Densité:
- Numéro de catalogue:CM986314
- Poids moléculaire:392.41
- 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.
- Benzofurans
- Benzofuran is an aromatic heterocyclic organic compound with the chemical formula C8H6O. It is a colorless oily liquid at room temperature with an aromatic odor. Benzofuran can be volatilized with water vapor and can be decomposed by potassium permanganate and other oxidants. It is an intermediate for the preparation of amiodarone and indene resin. Benzofuran derivatives are important pharmaceutical intermediates.
- Benzofuran | C8H6O | CID 9223 -Chemenu
- Benzofuran | C8H6O | CID 9223 |Where to Buy Benzofurans
- Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar.Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.