53555-10-5

Basic information

• Product Name: 1H-Isoindole-1,3(2H)-dione, 2-(4-methylphenyl)-4-nitro-
• CAS NO: 53555-10-5
• Molecular Formula: C15H10N2O4
• Molecular Weight: 282.255
• Mol File: 53555-10-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Isoindole-1,3(2H)-dione, 2-(4-methylphenyl)-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Isoindole-1,3(2H)-dione, 2-(4-methylphenyl)-4-nitro-(53555-10-5)
• EPA Substance Registry System: 1H-Isoindole-1,3(2H)-dione, 2-(4-methylphenyl)-4-nitro-(53555-10-5)

Safety Data

• Hazardous Substances Data: 53555-10-5(Hazardous Substances Data)

Upstream product

• 603-11-2 3-nitrophthalic acid 
• 106-49-0 p-toluidine 
• 641-70-3 3-nitrophthalic acid anhydride 
• 2272-45-9 benzal-p-toluidine 
• 88-99-3 benzene-1,2-dicarboxylic acid 
• 86-57-7 1-Nitronaphthalene 
• 24564-71-4 3-Nitrophthaloyl dichloride 

Downstream Products

• 1630974-77-4 acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester 
• 1630974-90-1 C₁₅H₁₂N₂O₄ 
• 1630974-74-1 2-(p-tolyl)-3-hydroxy-4-nitro-2,3-dihydroisoindol-1-one 
• 1630974-81-0 4-nitrobenzoic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester 
• 1630974-80-9 4-chlorobenzoic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester 
• 1630974-79-6 2,2-dimethylpropionic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester 
• 1630974-78-5 benzoic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester 

Relevant articles and documents

Mechanochemical synthesis of phthalimides with crystal structures of intermediates and products

A series of phthalimides have been successfully synthesized in the solid state by grinding (or kneading) of substituted phthalic anhydride and aniline derivatives. Selected products and intermediates were crystallized and characterized by crystallography leading to a potential rationale for the solid-state reactivity that suggests that co-crystals could serve as intermediates. This journal is

An expedient method to the synthesis of N-substituted 1H-isoindole-1,3(2H)- diones

The synthesis of N-substituted 1H-isoindole-1,3-(2H)-diones is described from the reaction of cyclic anhydrides with Schiff bases as suitable replacing substrates instead of the corresponding amines. The Japan Institute of Heterocyclic Chemistry.