31036-66-5

Basic information

• Product Name: 2,5-Pyrrolidinedione, 1-(3-nitrophenyl)-
• CAS NO: 31036-66-5
• Molecular Formula: C10H8N2O4
• Molecular Weight: 220.185
• Mol File: 31036-66-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,5-Pyrrolidinedione, 1-(3-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Pyrrolidinedione, 1-(3-nitrophenyl)-(31036-66-5)
• EPA Substance Registry System: 2,5-Pyrrolidinedione, 1-(3-nitrophenyl)-(31036-66-5)

Safety Data

• Hazardous Substances Data: 31036-66-5(Hazardous Substances Data)

Usage

General Description

2,5-Pyrrolidinedione, 1-(3-nitrophenyl)-, also known as 3-Nitrophenylpyrrolidinedione, is a chemical compound with the molecular formula C9H8N2O4. It is a yellow to brown crystalline powder that is used as a building block in the synthesis of pharmaceuticals and other organic compounds. This chemical is a versatile intermediate and has been studied for its potential applications in the field of drug discovery and development. It has also been used in the production of dyes, pigments, and other specialty chemicals. 3-Nitrophenylpyrrolidinedione is considered to be a potentially hazardous substance and should be handled with care, following proper safety precautions.

Upstream product

• 1797-93-9 3-(3-nitrophenylaminocarbonyl)propionic acid 
• 110-15-6 succinic acid 
• 99-09-2 3-nitro-aniline 
• 123-56-8 Succinimide 
• 13331-27-6 m-nitrobenzene boronic acid 
• 7300-93-8 N-(3-nitro-phenyl)-maleimide 
• 108-30-5 succinic acid anhydride 
• 42537-57-5 N-(3-nitrophenyl)maleamic acid 

Downstream Products

• 31036-67-6 N-m-Aminophenylsuccinimid 

Relevant articles and documents

Solvent-mediated one-pot synthesis of cyclic N-Substituted imides

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Three isomeric N-(nitrophenyl)succinimides: Isolated molecules, hydrogen-bonded sheets and a hydrogen-bonded three-dimensional framework

Molecules of N-(2-nitrophenyl)succinimide, C10H 8N2O4 are linked into sheets by a combination of C-H...O and C-H...π(arene) hydrogen bonds. Molecules of N-(3-nitrophenyl)succinimide are linked into a three-dimen

Cupric acetate mediated N-arylation by arylboronic acids: A preliminary investigation into the scope of application

A range of NH substrates of varying nucleophilicity were reacted with a selection of electronically diverse aryl boronic acids in the presence of cupric acetate in order to evaluate the generality of a previously described N-arylation procedure. The results of that investigation are discussed.