6-Bromoindoline is a chemical compound characterized by its indoline structure, which consists of a fused benzene and pyrrole ring system. The presence of a bromine atom at the 6-position of the indoline ring significantly influences its chemical properties and reactivity. This compound typically appears as a solid and is known for its potential applications in organic synthesis, medicinal chemistry, and as a building block in the development of pharmaceuticals. The bromine substituent can participate in various reactions, such as nucleophilic substitutions or cross-coupling reactions, making it a versatile intermediate in synthetic pathways. Additionally, 6-Bromoindoline may exhibit biological activity, which can be explored in drug discovery contexts. Its solubility and stability can vary depending on the solvent and conditions used, and it is important to handle this compound with care, following appropriate safety protocols due to the presence of bromine, which can be hazardous. Overall, 6-Bromoindoline is a valuable compound in both research and industrial applications.

6-Bromoindoline

63839-24-7: 6-Bromo-2,3-Dihydro-1H-Indole Hydrochloride, 1H-Indole, 6-bromo-2,3-dihydro-

6-Bromo-2,3-dihydro-1H-indole is a natural product that has been shown to inhibit cancer cell growth in vitro. In the presence of 6-bromoindole, cells are unable to proliferate and undergo apoptosis. This compound also shows anti-cancer activity against human leukemia cells. The mechanism of action for this molecule is not yet known but may be related to its ability to activate the caspase enzyme family or its ability to bind to DNA. 6-Bromoindole has been shown to have anti-inflammatory properties through inhibition of prostaglandin synthesis in animal models.

CAS 63839-24-7: 6-Bromoindoline

6-Bromo-2,3-dihydro-1H-indole

Ref: 3D-FB52114

6-Bromoindoline

Ref: 10-F092491

6-Bromo-2,3-dihydro-1H-indole

Ref: 54-OR305262