Nombre del producto:tert-butyl 3-bromospiro[5H-furo[3,4-b]pyridine-7,3'-azetidine]-1'-carboxylate

IUPAC Name:tert-butyl 3'-bromo-5'H-spiro[azetidine-3,7'-furo[3,4-b]pyridine]-1-carboxylate

CAS:1575836-59-7
Fórmula molecular:C14H17BrN2O3
Pureza:95%+
Número de catálogo:CM1017353
Peso molecular:341.21

Unidad de embalaje Stock disponible Precio($) Cantidad
CM1017353-100mg in stock ȁƀƀ
CM1017353-250mg in stock ǧɅNJ
CM1017353-500mg in stock NJƀȁț
CM1017353-1g in stock țNJɅǧ

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Detalles del producto

Núm. De CAS :1575836-59-7
Fórmula molecular:C14H17BrN2O3
Punto de fusión:-
Código de sonrisas:CC(C)(C)OC(=O)N1CC2(C1)C3=C(CO2)C=C(C=N3)Br
Densidad:
Número de catálogo:CM1017353
Peso molecular:341.21
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.
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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