Product Name:1-(5-Chloro-6-(2H-1,2,3-triazol-2-yl)pyridin-3-yl)-3-(2-methyl-7-morpholinothiazolo[5,4-b]pyridin-6-yl)urea

IUPAC Name:1-[5-chloro-6-(2H-1,2,3-triazol-2-yl)pyridin-3-yl]-3-[2-methyl-7-(morpholin-4-yl)-[1,3]thiazolo[5,4-b]pyridin-6-yl]urea

CAS:2178989-63-2
Molecular Formula:C19H18ClN9O2S
Purity:95%+
Catalog Number:CM558546
Molecular Weight:471.92

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Product Details

CAS NO:2178989-63-2
Molecular Formula:C19H18ClN9O2S
Melting Point:-
Smiles Code:O=C(NC1=CN=C(SC(C)=N2)C2=C1N3CCOCC3)NC4=CC(Cl)=C(N5N=CC=N5)N=C4
Density:
Catalog Number:CM558546
Molecular Weight:471.92
Boiling Point:
MDL No:
Storage:

Category Infos

Morpholines
Morpholine contains secondary amine groups and has all the typical reactive characteristics of secondary amine groups. It can react with inorganic acids to form salts, and react with organic acids to form salts or amides, which can be subjected to alkylation reaction, and can also be reacted with ethylene oxide, ketone or Willgerodt reaction. Morpholine is a six-membered ring containing oxygen and nitrogen, and its alkalinity is much lower than that of its parent piperidine. The marketed morpholine drugs are mainly distributed in the fields of tumors, cardiovascular and cerebrovascular diseases, respiratory system diseases, digestive system diseases, infectious diseases and mental disorders.
morpholine price
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Triazoles
Triazole refers to a heterocyclic compound with the molecular formula C2H3N3, which has a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease already affect many people around the world, and these numbers are increasing rapidly. Treatment for these disorders is often aimed at relieving symptoms and has no cure. Research on new molecules is underway, and heterocyclic compounds have important pharmacological implications. Triazoles and tetrazoles are emerging as new molecules in this field.
Thiazolopyridines
Thiazolopyridines are a class of heterocyclic compounds. Thiazolopyridines were developed as allosteric inhibitors of MALT1 with good cellular potency and refined selectivity.