55862-98-1

Basic information

• Product Name: 1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione
• Synonyms: 1H-pyrrole-2,5-dione, 1-(2,4,6-trimethylphenyl)-; 1-Mesityl-1H-pyrrole-2,5-dione
• CAS NO: 55862-98-1
• Molecular Formula: C₁₃H₁₃NO₂
• Molecular Weight: 215.2478
• Mol File: 55862-98-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 353°C at 760 mmHg
• Flash Point: 156.1°C
• Density: 1.201g/cm³
• Vapor Pressure: 3.7E-05mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: 1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione(55862-98-1)
• EPA Substance Registry System: 1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione(55862-98-1)

Safety Data

• Hazardous Substances Data: 55862-98-1(Hazardous Substances Data)

Usage

General Description

1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione, also known as trimethylphenylpyrrole, is a chemical compound with the molecular formula C13H11NO2. It is a heterocyclic aromatic compound that contains a pyrrole ring with three methyl groups attached to the phenyl ring. Trimethylphenylpyrrole has been studied for its potential applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its unique chemical structure and properties make it a promising candidate for use in various electronic devices and materials. Additionally, it may have potential pharmaceutical applications due to its interesting molecular structure and biological activity.

Upstream product

• 88-05-1 2,4,6-trimethylaniline 
• 189875-67-0 C₁₃H₁₅NO₃ 

Downstream Products

• 1158819-14-7 C₁₈H₁₇NO₅ 
• 1513872-37-1 N-(N-2,4,6-trimethylphenylsuccinimidyl)-amphotericin B 

Relevant articles and documents

Efficient method for the synthesis of functionalized basic maleimides

A three-step procedure involving Diels-Alder condensation of maleic anhydride with furane, formation of N-substituted imide upon reaction with appropriate diamine, and a final retro Diels-Alder regeneration of the maleic carbon-carbon double bond is proposed for an unequivocal synthesis of N-substituted basic maleimides. The novel method is characterized by mild reaction conditions, easy work-up, high yields, and no need for additional catalysis.

N-phenyl maleic imides

Fungicidal compositions, optionally contain chlorinated N- (2,4,6-trimethhenyl)-maleic imides as active material. Such materials find use for controlling fungus disease in plants, especially in agriculture, viticulture, arboriculture, market-gardening an