Nombre del producto:N-(1H-indazol-6-yl)-2-(thiophene-2-amido)-1,3-oxazole-4-carboxamide

IUPAC Name:N-(1H-indazol-6-yl)-2-(thiophene-2-amido)-1,3-oxazole-4-carboxamide

CAS:1396710-33-0
Fórmula molecular:C16H11N5O3S
Pureza:95%+
Número de catálogo:CM940106
Peso molecular:353.36

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Detalles del producto

Núm. De CAS :1396710-33-0
Fórmula molecular:C16H11N5O3S
Punto de fusión:-
Código de sonrisas:O=C(NC1=NC(=CO1)C(=O)NC1=CC=C2C=NNC2=C1)C1=CC=CS1
Densidad:
Número de catálogo:CM940106
Peso molecular:353.36
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
Oxazoles
Oxazoles are heterocyclic aromatic compounds containing one oxygen atom and one nitrogen atom, separated by a carbon atom. The presence of two heteroatoms (oxygen and nitrogen) provides possible interactions (hydrogen, hydrophobic, van der Waals or dipole bonds) with a wide range of receptors and enzymes. Oxazole rings are valuable heterocyclic scaffolds for the design of novel therapeutics with anticancer, antiviral, antibacterial, anti-inflammatory, neuroprotective, antidiabetic, and antidepressant properties due to their wide range of targets and biological activities.
Indazoles
Indazoles are a class of organic heterocyclic compounds, also known as 1,2-diazaindene and benzopyrazole. Indazole is a good bioisomer of phenol, which is more lipophilic than phenol and less prone to phase I and II metabolism. Indazole derivatives have a wide range of biological activities, and it has been confirmed that indazole compounds have anti-tumor, analgesic, anti-inflammatory and other drug activities. Anticancer is the most important application field of indazole drugs. Renal cell carcinoma, solid tumor, nausea and vomiting caused by chemotherapy and leukemia are the main indications of this structural backbone drug.

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