cas 1396678-26-4|| where to buy N-{5-[1-(4-chlorophenyl)-5-oxopyrrolidine-3-carbonyl]-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-yl}-5-methyl-1,2-oxazole-3-carboxamide

Product Name:N-{5-[1-(4-chlorophenyl)-5-oxopyrrolidine-3-carbonyl]-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-yl}-5-methyl-1,2-oxazole-3-carboxamide

IUPAC Name:N-{5-[1-(4-chlorophenyl)-5-oxopyrrolidine-3-carbonyl]-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-yl}-5-methyl-1,2-oxazole-3-carboxamide

: CAS：1396678-26-4; Molecular Formula：C22H20ClN5O4S; Purity：95%+

: Catalog Number：CM1001661; Molecular Weight：485.94

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: CAS NO:1396678-26-4; Molecular Formula:C22H20ClN5O4S; Melting Point:-; Smiles Code:CC1=CC(=NO1)C(=O)NC1=NC2=C(CN(CC2)C(=O)C2CN(C(=O)C2)C2=CC=C(Cl)C=C2)S1; Density:

: Catalog Number:CM1001661; Molecular Weight:485.94; Boiling Point:; MDL No:; Storage:

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: Thiazoles; Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.

: Pyrrolidines; Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.

: 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.

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