Home Chemistry Heterocyclic Building Blocks Indolines (E)-[3,3'-Biindolinylidene]-2,2'-Dione
Nucleophilic Addition: Isatin can undergo nucleophilic addition reactions with compounds like amines or hydrazines. This can lead to the formation of a variety of derivatives, such as isatin hydrazones and isatin semicarbazones.
Ring Closure Reactions: Isatin can be involved in ring closure reactions. For example, it can undergo intramolecular cyclization with hydrazines to form indole derivatives.
Condensation Reactions: Isatin can be condensed with various reagents, such as carbonyl compounds or amines, to produce a range of products, including oxindole derivatives.
Oxidation Reactions: Isatin can be oxidized to produce various products, including isatins with additional functional groups.
Reduction Reactions: Isatin can be reduced to yield compounds such as 3-hydroxyindolin-2-one.
Mannich Reactions: Isatin can participate in Mannich reactions, which involve the condensation of isatin with a primary or secondary amine and formaldehyde to form various substituted isatin derivatives.
Friedel-Crafts Acylation: Isatin can undergo Friedel-Crafts acylation reactions with various acylating agents to introduce acyl groups into the isatin ring system.
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(E)-6,6'-Dibromo-[3,3'-biindolinylidene]-2,2'-dione
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(E)-6,6'-Dibromo-[3,3'-biindolinylidene]-2,2'-dione
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(E)-6-Bromo-3-(6-bromo-1-(2-octyldodecyl)-2-oxoindolin-3-ylidene)-1-(2-octyldodecyl)indolin-2-one
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