1447998-83-5

Basic information

• Product Name: 3-benzyl-3-(5-nitro-1-H-indol-3-yl)-2-phenylisoindolin-1-one
• Synonyms: 3-benzyl-3-(5-nitro-1-H-indol-3-yl)-2-phenylisoindolin-1-one
• CAS NO: 1447998-83-5
• Molecular Weight: 459.504
• Mol File: 1447998-83-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-benzyl-3-(5-nitro-1-H-indol-3-yl)-2-phenylisoindolin-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzyl-3-(5-nitro-1-H-indol-3-yl)-2-phenylisoindolin-1-one(1447998-83-5)
• EPA Substance Registry System: 3-benzyl-3-(5-nitro-1-H-indol-3-yl)-2-phenylisoindolin-1-one(1447998-83-5)

Safety Data

• Hazardous Substances Data: 1447998-83-5(Hazardous Substances Data)

Upstream product

• 10282-57-2 2-bromobenzanilide 
• 6146-52-7 5-nitroindole 
• 536-74-3 phenylacetylene 
• 15310-01-7 benodanil 

Relevant articles and documents

Nanodomain cubic cuprous oxide as reusable catalyst in one-pot synthesis of 3-alkyl/aryl-3-(pyrrole-2-yl/indole-3-yl)-2-phenyl-2,3-dihydro-isoindolinones in aqueous medium

An environmentally benign one-pot protocol has been developed for the syntheses of 3-alkyl/aryl-3-(pyrrole/indole-2/3-yl)-2-phenyl-2,3-dihydro- isoindolinones via a multi-component one-pot reaction involving 2-iodo-N-phenylbenzamides, terminal alkyne and substituted indoles/pyrroles in aqueous medium using cubic cuprous oxide nanoparticles as catalyst. It involves domino Sonogashira-5-exo-dig-cyclization followed by regioselective nucleophilic addition of indoles or pyrroles, in aqueous medium without using any surfactants or additional ligands. The Royal Society of Chemistry 2014.