7143-61-5 Usage
Uses
Used in Organic Synthesis:
2,6-Bis(3-methylphenyl)pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone is used as a key intermediate in organic synthesis for the development of new compounds with potential applications in various industries.
Used in Material Sciences:
In the field of material sciences, 2,6-Bis(3-methylphenyl)pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone is used as a precursor for creating advanced materials with unique properties.
Used in Pharmaceutical Development:
2,6-Bis(3-methylphenyl)pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone is used as a lead compound in pharmaceutical research for its antioxidant and antimicrobial activities, which could contribute to the development of new drugs and bioactive materials.
Used in Organic Electronic Devices:
Due to its structure, 2,6-Bis(3-methylphenyl)pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone is used in the development of organic electronic devices, where its properties can enhance device performance.
Used in Nano and Micro-scale Technologies:
2,6-Bis(3-methylphenyl)pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone's potential as a functional material makes it suitable for use in various nano and micro-scale technologies, where it can contribute to the advancement of miniaturized devices and systems.
Check Digit Verification of cas no
The CAS Registry Mumber 7143-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7143-61:
(6*7)+(5*1)+(4*4)+(3*3)+(2*6)+(1*1)=85
85 % 10 = 5
So 7143-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H16N2O4/c1-13-5-3-7-15(9-13)25-21(27)17-11-19-20(12-18(17)22(25)28)24(30)26(23(19)29)16-8-4-6-14(2)10-16/h3-12H,1-2H3
7143-61-5Relevant academic research and scientific papers
Preparation of imides
-
, (2008/06/13)
Cyclic imides are prepared by reacting carbon monoxide with an ortho dihalide aromatic compound or a cis-1,2-vinyl dihalide and an amide in the presence of palladium catalyst and a base. The process is preferably conducted in the presence of a dipolar aprotic solvent as a liquid reaction medium.
