5,7-Dichloroisatin is an organic compound characterized by its structure, which includes a fused isatin framework with two chlorine substituents at the 5 and 7 positions of the indole ring. This compound typically appears as a yellow to orange crystalline solid and is known for its potential biological activities, including antimicrobial and anticancer properties. The presence of chlorine atoms enhances its reactivity and may influence its interaction with biological targets. 5,7-Dichloroisatin is soluble in organic solvents, such as dimethyl sulfoxide (DMSO) and ethanol, but has limited solubility in water. Its molecular formula reflects the presence of carbon, hydrogen, nitrogen, and chlorine, contributing to its unique chemical behavior. The compound is often utilized in synthetic organic chemistry as an intermediate for the development of various pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as with many halogenated organic substances, due to potential toxicity and environmental concerns.

5,7-Dichloroisatin

6374-92-1: 1H-Indole-2,3-dione, 5,7-dichloro-, 228-928-3, 5,7-Dichloro-1H-indole-2,3-dione, Indole-2,3-dione, 5,7-dichloro-, Isatin, 5,7-dichloro-, NSC 26045, 5,7-Dichloroisatin

5,7-Dichloroisatin is a synthetic compound which has been shown to have antitumor effects on animals. It is an analog of epoxydes and has been synthesized by reacting morpholine with dichloroisatin. 5,7-Dichloroisatin also undergoes ring-opening and dehydrogenation reactions in acetonitrile to yield the corresponding epoxides. This compound is resistant to piperidine and anhydrous acetonitrile, but isomerizes with chloride and reacts with mismatched anhydride.

CAS 6374-92-1: 5,7-Dichloroisatin

5,7-Dichloroisatin

Ref: 3D-FD149500

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

Ref: 54-OR94464

5,7-Dichloroindoline-2,3-dione

Ref: IN-DA003MAO

5,7-Dichloroisatin

Ref: 10-F045004