5,7-Dibromoisatin is a synthetic organic compound belonging to the isatin family, characterized by its unique brominated structure. It features two bromine atoms substituted at the 5 and 7 positions of the isatin core, which is a bicyclic compound containing both a ketone and an amine functional group. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. 5,7-Dibromoisatin is known for its potential biological activities, including antimicrobial and anticancer properties, making it of interest in medicinal chemistry. Its reactivity is influenced by the presence of the bromine substituents, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound's solubility can vary in different solvents, affecting its application in various chemical processes. As with many brominated compounds, safety precautions should be taken due to potential toxicity and environmental concerns associated with bromine-containing substances.

5,7-Dibromoisatin

6374-91-0: 5,7-Dibromo-1H-indole-2,3-dione, 5,7-Dibromoisatin, Indole-2,3-dione, 5,7-dibromo-, Isatin, 5,7-dibromo-, Scr 0009418, 1H-Indole-2,3-dione, 5,7-dibromo-

5,7-Dibromoindoline-2,3-dione

5,7-Dibromo-1H-indole-2,3-dione is a selenium compound that has been synthesized to be used as an analog of vinblastine. It has anti-cancer activities and has been shown to inhibit the growth of primary tumor cells in mice. 5,7-Dibromo-1H-indole-2,3-dione also has pharmacokinetic properties that are similar to those of vinblastine sulfate. This compound can be used in cancer research as a test compound for assessing anticancer activity.

CAS 6374-91-0: 5,7-Dibromoisatin

5,7-Dibromoindoline-2,3-dione

Ref: IN-DA003MAI

5,7-Dibromoindoline-2,3-dione

Ref: 10-F336739

5,7-Dibromo-1H-indole-2,3-dione

Ref: 3D-FD124001

5,7-Dibromoindoline-2,3-dione

Ref: 54-OR74595