87243-31-0

Basic information

• Product Name: 2-(4-bromophenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione
• Synonyms: 2-(4-bromophenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione
• CAS NO: 87243-31-0
• Molecular Weight: 352.187
• Mol File: 87243-31-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(4-bromophenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromophenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione(87243-31-0)
• EPA Substance Registry System: 2-(4-bromophenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione(87243-31-0)

Safety Data

• Hazardous Substances Data: 87243-31-0(Hazardous Substances Data)

Upstream product

• 81-84-5 1,8-Naphthalic anhydride 
• 106-40-1 4-bromo-aniline 
• 81-83-4 1,8-Naphthalimide 
• 65826-67-7 bis(4-bromophenyl)iodonium bromide 

Relevant articles and documents

Copper-catalyzed direct N-arylation of naphthalimides using diaryliodonium Salts

An effective copper-catalyzed N-arylation of naphthal-imides with diaryliodonium salts in toluene at 100 °C has been developed. This cross-coupling reaction gives the desired N-arylated 1,8-naphthalimides in moderate to good yields. The synthetic potentia

N-SUBSTITUTED ISONAPHTHALIMIDES. FORMATION AND REACTION WITH AMINES

N-Substituted isonaphthalimides and N-substituted naphthalimides, as considered previously, are formed in the reaction of 1,8-naphthaloyl chloride with primary amines.The reaction of N-substituted isonaphthalimides with sterically unhindered amines leads to the N,N'-substituted diamides of 1,8-naphthalenedicarboxylic acid.In the case of sterically hindered amines it results in isomerization to the N-substituted naphthalimides.The thermolysis of the N,N'-substituted diamides of 1,8-naphthalenedicarboxylic acid leads to amines and N-substituted naphthalimides.