55862-98-1 Usage
Description
1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione, also known as trimethylphenylpyrrole, is a heterocyclic aromatic compound with the molecular formula C13H11NO2. It features a pyrrole ring and a phenyl ring with three methyl groups attached, giving it unique chemical properties and potential applications in various fields.
Uses
Used in Organic Electronics:
1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione is used as a component in organic electronics for its potential applications in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its unique chemical structure and properties make it a promising candidate for enhancing the performance of these electronic devices and materials.
Used in Pharmaceutical Applications:
1-(2,4,6-trimethylphenyl)-1H-pyrrole-2,5-dione may be utilized as a pharmaceutical compound due to its interesting molecular structure and potential biological activity. Further research and development could reveal its use in the creation of new drugs or therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 55862-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55862-98:
(7*5)+(6*5)+(5*8)+(4*6)+(3*2)+(2*9)+(1*8)=161
161 % 10 = 1
So 55862-98-1 is a valid CAS Registry Number.
55862-98-1Relevant articles and documents
Efficient method for the synthesis of functionalized basic maleimides
Salewska, Natalia,Milewska, Maria J.
, p. 999 - 1003 (2014/08/05)
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
-
, (2008/06/13)
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