Nombre del producto:4-(phenoxymethyl)-1-{1-[4-(1,3-thiazol-2-yloxy)benzoyl]azetidin-3-yl}-1H-1,2,3-triazole

IUPAC Name:4-(phenoxymethyl)-1-{1-[4-(1,3-thiazol-2-yloxy)benzoyl]azetidin-3-yl}-1H-1,2,3-triazole

CAS:2034592-44-2
Fórmula molecular:C22H19N5O3S
Pureza:95%+
Número de catálogo:CM883698
Peso molecular:433.49

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Detalles del producto

Núm. De CAS :2034592-44-2
Fórmula molecular:C22H19N5O3S
Punto de fusión:-
Código de sonrisas:O=C(N1CC(C1)N1C=C(COC2=CC=CC=C2)N=N1)C1=CC=C(OC2=NC=CS2)C=C1
Densidad:
Número de catálogo:CM883698
Peso molecular:433.49
Punto de ebullición:
Nº Mdl:
Almacenamiento:

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.
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.
Azetidines
Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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