CAS 183208-35-7
:5-Brom-1H-pyrrolo[2,3-b]pyridin
- 1H-Pyrrolo[2,3-b]pyridine, 5-bromo-
- 5-Bromo azaindole
- 5-Bromo-1H-Pyrrolo[2,3-B]Pyridine
- 5-Bromo-1H-pyrrolo2,3-büpyridine
- 5-Bromo-7H-pyrrolo[2,3-b]pyridine
- 5-Bromo-7-azaindole
5-Bromo-1H-pyrrolo[2,3-b]pyridine
CAS:Formel:C7H5BrN2Reinheit:>98.0%(GC)(T)Farbe und Form:White to Yellow to Orange powder to crystalMolekulargewicht:197.045-Bromo-7-azaindole, 96%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formel:C7H5BrN2Reinheit:96%Molekulargewicht:197.041H-Pyrrolo[2,3-b]pyridine, 5-bromo-
CAS:Formel:C7H5BrN2Reinheit:98%Farbe und Form:SolidMolekulargewicht:197.03205-Bromo-7-azaindole
CAS:5-Bromo-7-azaindoleFormel:C7H5BrN2Reinheit:98%Farbe und Form: off white crystalline solidMolekulargewicht:197.03g/mol5-Bromo-7-azaindole
CAS:5-Bromo-7-azaindole is a nitrogen heterocycle that has shown promising anti-cancer properties. This compound is synthesized by the reaction of sodium azide and 5-bromo-2,4,6-trinitrobenzene in anhydrous conditions. 5-Bromo-7-azaindole displays significant cytotoxicity against human ovarian carcinoma cells in vivo and inhibits the proliferation of cancer cells by binding to ATP synthase. The anticancer activity of this compound is due to its ability to inhibit the synthesis of DNA and RNA, which are vital for cell division. 5-Bromo-7-azaindole also shows an increase in hydrogen bonding, which can be used to explain its structural analysis.
Formel:C7H5BrN2Reinheit:Min. 98 Area-%Farbe und Form:PowderMolekulargewicht:197.03 g/mol5-Bromo-1H-pyrrolo[2,3-b]pyridine
CAS:Formel:C7H5BrN2Reinheit:95%Farbe und Form:Light yellow powderMolekulargewicht:197.035







