Nom du produit:N-(5-methyl-1,2-oxazol-3-yl)-4-{[2-methyl-7-(trifluoromethyl)quinolin-4-yl]amino}benzene-1-sulfonamide
IUPAC Name:N-(5-methyl-1,2-oxazol-3-yl)-4-{[2-methyl-7-(trifluoromethyl)quinolin-4-yl]amino}benzene-1-sulfonamide
- CAS:882253-03-4
- Formule moléculaire:C21H17F3N4O3S
- Pureté:95%+
- Numéro de catalogue:CM961953
- Poids moléculaire:462.45
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Détails du produit
- N° CAS:882253-03-4
- Formule moléculaire:C21H17F3N4O3S
- Point de fusion:-
- Code SMILES:CC1=CC(NS(=O)(=O)C2=CC=C(NC3=C4C=CC(=CC4=NC(C)=C3)C(F)(F)F)C=C2)=NO1
- Densité:
- Numéro de catalogue:CM961953
- Poids moléculaire:462.45
- 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.
- Isoxazoles
- Isoxazole is a liquid heterocyclic compound C3H3NO isomeric with oxazole and having a penetrating odor like that of pyridine. Isoxazoles belong to an important class of five-membered aromatic heterocycles containing two electronegative heteroatoms, nitrogen and oxygen, in a 1,2-relationship and three regular sp2 carbon atoms. These molecules are found to be key components in various synthetic products in daily use and also present as a pharmacophore essential for biological activity in many drugs and bioactive natural products. In addition, isoxazoles have demonstrated their ability to exhibit hydrogen bond donor/acceptor interactions with a variety of enzymes and receptors.