Nombre del producto:tert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate

IUPAC Name:tert-butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate

CAS:1299607-55-8
Fórmula molecular:C11H12BrN3O2
Pureza:95%
Número de catálogo:CM151955
Peso molecular:298.14

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CM151955-250mg in stock ŵȡ
CM151955-1g in stock ƛƥũ
CM151955-5g in stock Ȑƿƥ

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Detalles del producto

Núm. De CAS :1299607-55-8
Fórmula molecular:C11H12BrN3O2
Punto de fusión:-
Código de sonrisas:O=C(N1N=CC2=CC(Br)=CN=C21)OC(C)(C)C
Densidad:
Número de catálogo:CM151955
Peso molecular:298.14
Punto de ebullición:
Nº Mdl:MFCD18803503
Almacenamiento:

Category Infos

Pyrazolopyridines
Over the past few years, many pyrazole fused-ring systems, especially with applications in medicinal chemistry, have been published. These include general structures such as pyrazoline, pyrazoline, pyrazoquinoline, pyrazoloisoquinoline, pyrazoline, pyrazolopyrazine, pyrazolopyrazine, pyranopyrazole, pyrano Pyrazoles, pyrazolotriazines and pyrazole fused phosphorus rings.

Column Infos

Olverembatinib
Ascentage Pharma announced that updated results from three studies of olverembatinib, have been released in posters at the 2024 European Hematology Association Hybrid Congress, taking place in Madrid, Spain.
Olverembatinib (HQP1351) is an oral, third-generation BCR-ABL1 tyrosine kinase inhibitor (TKI) developed by Ascentage Pharma for the treatment of chronic myeloid leukaemia (CML), acute myeloid leukaemia, acute lymphoblastic leukaemia (ALL) and solid tumours, including gastrointestinal stromal tumours (GIST). Olverembatinib is an ATP binding-site inhibitor of wild type BCR-ABL1 kinase and a broad spectrum of BCR-ABL1 mutants, including mutant T315I, which confers resistance against all first- and second-generation TKIs. 

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