123299-02-5

Basic information

• Product Name: 2-{4-[4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,7-diphenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione
• CAS NO: 123299-02-5
• Molecular Weight: 564.64
• Mol File: 123299-02-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-{4-[4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,7-diphenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{4-[4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,7-diphenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione(123299-02-5)
• EPA Substance Registry System: 2-{4-[4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,7-diphenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione(123299-02-5)

Safety Data

• Hazardous Substances Data: 123299-02-5(Hazardous Substances Data)

Upstream product

• 886-65-7 trans,trans-1,4-Diphenyl-1,3-butadiene 
• 13676-54-5 1,1'-(methylenedi-4,1-phenylene)bismaleimide 
• 5471-63-6 1,3-diphenylisobenzofuran 

Relevant articles and documents

N,N'-DIMALEIMIDES IN THE DIELS-ALDER REACTION. I. KINETICS OF THE UNCATALYZED REACTION WITH trans,trans-1,4-DIPHENYLBUTADIENE AND 1,3-DIPHENYLISOBENZOFURAN

The kinetic behavior of a series of diimides, in which the maleimide rings are linked through various bridges, in the Diels-Alder reaction with trans,trans-1,4-diphenylbutadiene and 1,3-diphenylisobenzofuran was studied.The energies of charge transfer were determined and the electron affinities were calculated by spectrophotometry of the charge-transfer complexes between the imides and hexamethylbenzene.Although the rates of reaction of the bisimides with the investigated dienes differ by seven orders of magnitude, the general type of "diene-donor, dienophile-acceptor" reaction is preserved.