Product Name:N-[4-(1,3-benzothiazol-2-yl)-1,3-thiazol-2-yl]-3-oxo-3H-benzo[f]chromene-2-carboxamide

IUPAC Name:N-[4-(1,3-benzothiazol-2-yl)-1,3-thiazol-2-yl]-3-oxo-3H-benzo[f]chromene-2-carboxamide

CAS:477538-99-1
Molecular Formula:C24H13N3O3S2
Purity:95%+
Catalog Number:CM989493
Molecular Weight:455.51

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Product Details

CAS NO:477538-99-1
Molecular Formula:C24H13N3O3S2
Melting Point:-
Smiles Code:O=C(NC1=NC(=CS1)C1=NC2=CC=CC=C2S1)C1=CC2=C(OC1=O)C=CC1=C2C=CC=C1
Density:
Catalog Number:CM989493
Molecular Weight:455.51
Boiling Point:
MDL No:
Storage:

Category Infos

Benzothiazoles
Benzothiazoles are aromatic heterocyclic compounds with the chemical formula C7H5NS. Benzothiazoles and their derivatives are a very important class of heterocyclic compounds that are ubiquitous in nature and are mainly used in medicine, agriculture and industry. In medicine, benzothiazole derivatives are a kind of very important pharmaceutical intermediates with good pharmacological and biological activities. It can be used as a fungicide, anti-tuberculosis drug, anti-malarial, anti-convulsant, insecticide, sedative and anti-inflammatory drug, and can also be used to treat diabetes and has anti-cancer effects.
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.