6-Bromo-5-chloro-1H-indole-2,3-dione, with the CAS number 192799-05-6, is a synthetic organic compound that belongs to the indole family, characterized by its fused bicyclic structure. This compound features both bromine and chlorine substituents, which contribute to its unique reactivity and potential applications in medicinal chemistry. The presence of the dione functional groups indicates that it can participate in various chemical reactions, such as nucleophilic additions and cycloadditions. Its molecular structure suggests that it may exhibit biological activity, making it of interest in drug discovery and development. Additionally, the halogen substituents can influence the compound's solubility, stability, and interaction with biological targets. As with many indole derivatives, this compound may also exhibit fluorescence properties, which can be useful in analytical applications. Overall, 6-Bromo-5-chloro-1H-indole-2,3-dione is a versatile compound with potential implications in both research and pharmaceutical contexts.

6-Bromo-5-chloro-1H-indole-2,3-dione

6-Bromo-5-chloroindoline-2,3-dione

1H-Indole-2,3-dione, 6-bromo-5-chloro-

6-Bromo-5-chloro-1H-indole-2,3-dione is a monomer that can be used in the production of solar cells or devices. It has been shown to be an electron donor and is capable of donating electrons to other molecules. This chemical compound also participates in polymerizing reactions. 6-Bromo-5-chloro-1H-indole-2,3-dione is a polyaromatic compound that has been shown to form polymers with phenylene and vinylene groups.

CAS 192799-05-6: 6-Bromo-5-chloro-1H-indole-2,3-dione

6-Bromo-5-chloroindoline-2,3-dione

Ref: 54-OR52245

6-Bromo-5-chloro-1H-indole-2,3-dione

Ref: TR-B682150

6-Bromo-5-chloroindoline-2,3-dione

Ref: 10-F233115

1H-Indole-2,3-dione, 6-bromo-5-chloro-

Ref: IN-DA002GAQ

6-Bromo-5-chloro-1H-indole-2,3-dione

Ref: 3D-FB19154