CAS 183208-35-7
:5-Bromo-1H-pyrrolo[2,3-b]pyridine
- 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 :Formule :C7H5BrN2Degré de pureté :>98.0%(GC)(T)Couleur et forme :White to Yellow to Orange powder to crystalMasse moléculaire :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
Formule :C7H5BrN2Degré de pureté :96%Masse moléculaire :197.041H-Pyrrolo[2,3-b]pyridine, 5-bromo-
CAS :Formule :C7H5BrN2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :197.03205-Bromo-7-azaindole
CAS :5-Bromo-7-azaindoleFormule :C7H5BrN2Degré de pureté :98%Couleur et forme : off white crystalline solidMasse moléculaire :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.
Formule :C7H5BrN2Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :197.03 g/mol5-Bromo-1H-pyrrolo[2,3-b]pyridine
CAS :Formule :C7H5BrN2Degré de pureté :95%Couleur et forme :Light yellow powderMasse moléculaire :197.035







