Product Name:N-(2-oxo-2H-chromen-3-yl)-2-(pyrazin-2-yl)-1,3-thiazole-4-carboxamide

IUPAC Name:N-(2-oxo-2H-chromen-3-yl)-2-(pyrazin-2-yl)-1,3-thiazole-4-carboxamide

CAS:1226453-37-7
Molecular Formula:C17H10N4O3S
Purity:95%+
Catalog Number:CM950286
Molecular Weight:350.35

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Product Details

CAS NO:1226453-37-7
Molecular Formula:C17H10N4O3S
Melting Point:-
Smiles Code:O=C(NC1=CC2=CC=CC=C2OC1=O)C1=CSC(=N1)C1=CN=CC=N1
Density:
Catalog Number:CM950286
Molecular Weight:350.35
Boiling Point:
MDL No:
Storage:

Category Infos

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.
Pyrazines
Pyrazine is a heterocyclic aromatic organic compound with chemical formula C4H4N2. The marketed pyrazine drugs are mainly distributed in the field of anti-tumor and anti-infection. In recent years, there have been many new drugs in various fields, and there are some new target drugs worthy of attention.
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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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