72677-30-6

Usage

Indole

A bicyclic compound with a benzene ring fused to a pyrrole ring.

Amide

A functional group with a carbonyl group (C=O) bonded to a nitrogen atom (-NH2).

Isoindole

A tricyclic compound with a benzene ring fused to a pyridine ring.
4. Potential applications in pharmaceuticals and organic synthesis
The compound's unique structure and properties may make it useful in the development of new drugs and as a building block for synthesizing other complex organic compounds.
5. Building block for synthesis of other complex organic compounds
Due to its heterocyclic nature and various functional groups, 2-[(2-oxo-2H-indol-3-yl)amino]-1H-isoindole-1,3(2H)-dione can be used as a starting point for creating more complex molecules with diverse applications.
6. Starting material for the development of new drugs
The compound's structure may provide a foundation for researchers to create new pharmaceuticals with specific therapeutic effects.
7. Need for further research and study
To fully understand the potential uses and properties of 2-[(2-oxo-2H-indol-3-yl)amino]-1H-isoindole-1,3(2H)-dione, additional research and investigation are required.

Upstream product

• 91-56-5 indole-2,3-dione 
• 1875-48-5 N-aminophthalamide 
• 85-44-9 phthalic anhydride 
• 2365-44-8 3-hydrazonoindolin-2-one 

Relevant academic research and scientific papers

N-aminophthalimide as a synthon for heterocyclic schiff bases: Efficient utilization as corrosion inhibitors of mild steel in 0.5 mol.L-1 H2SO4 solution

MANY Schiff bases were prepared to inhibit the corrosion reactions of mild steel in acidic medium. Their chemical structures were determined by using different techniques. Thermodynamic adsorption parameters of inhibitors were determined using the Langmui

Synthesis of some new mixed azines, Schiff and Mannich bases of pharmaceutical interest related to isatin

The mixed azines 3a-h and 4 were obtained by treating 3-hydrazonoindolin-2-one (2) with the appropriate aldehyde or dialdehyde. Treatment of 3b or 3c with formaldehyde or glutaric dialdehyde and the appropriate amine afforded the azine Mannich bases 5-7. The condensation of isatin or its N-Mannich base 8 with 1-aminopiperidine, 4-aminomorpholine and 1,4-diaminopiperazine gave 10a- d, 12 and 13. The Mannich bases 14 and 15 were obtained from 10a and 10b. Treatment of 2 with succinic, phthalic and quinolinic anhydride and pyromellitic dianhydride afforded compounds 16, 17a, 17b and 18, respectively. The synthesis of isatin Schiff bases incorporating a benzoylpiperidine, benzoylmorpholine and 1,4-dibezoylpiperazine moiety and their N-Mannich bases was investigated.

Synthesis, antiviral and antimicrobial screening of some new 2-oxoindoline derivatives

New 3-(2-(5-(aryldiazenyl)-4-methylthiazol-2-yl)hydrazono)indolin-2-ones were prepared by the reaction of isatin β-thiosemicarbazone with different hydrazonoyl chlorides. Imide derivatives were prepared by the reaction of isatin hydrazone with various anh