5,6-Dichloroindole is a chemical compound characterized by the presence of two chlorine atoms attached to the indole structure at the 5 and 6 positions. This compound belongs to the class of heterocyclic aromatic compounds, which are known for their stability and unique electronic properties due to the presence of nitrogen in the ring. 5,6-Dichloroindole is typically a solid at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics. It is often used in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of chlorine substituents can influence the compound's reactivity, making it a valuable building block in medicinal chemistry. Additionally, the indole moiety is known for its biological significance, as many indole derivatives exhibit a range of biological activities, including antimicrobial and anticancer properties. Safety data should be consulted for handling and usage, as halogenated compounds can pose environmental and health risks.

5,6-Dichloroindole

1H-Indole, 5,6-dichloro-

5,6-Dichloro-1H-indole

5,6-Dichloroindole is a chemical compound that contains a functional group with acidic properties. The compound has been shown to inhibit the activity of bafilomycin A1, which is an inhibitor of vacuolar ATPase. This inhibition leads to an increase in intracellular phosphate levels and an accumulation of lysosomal membrane proteins. 5,6-Dichloroindole has also been found to inhibit bone resorption in gramine-fed rats. It also has anti-inflammatory effects and inhibits the growth of zoobotryon pinnatum cells and algal cells. 5,6-Dichloroindole can be used as a molecular descriptor for predicting the presence or absence of bryozoan species in a sample.

CAS 121859-57-2: 5,6-Dichloroindole

1H-Indole, 5,6-dichloro-

Ref: IN-DA001652

5,6-Dichloroindole

Ref: 10-F093048

5,6-Dichloro-1H-indole

Ref: 54-OR15747

5,6-Dichloroindole

Ref: 3B-D4924

5,6-Dichloroindole

Ref: 3D-FD31359