7685-88-3

Basic information

• Product Name: 1-Phenyl-3-[(phenylmethyl)amino]-2,5-pyrrolidinedione
• Synonyms: 1-Phenyl-3-[(phenylmethyl)amino]-2,5-pyrrolidinedione
• CAS NO: 7685-88-3
• Molecular Formula: C₁₇H₁₆N₂O₂
• Molecular Weight: 280.32114
• Mol File: 7685-88-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Phenyl-3-[(phenylmethyl)amino]-2,5-pyrrolidinedione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phenyl-3-[(phenylmethyl)amino]-2,5-pyrrolidinedione(7685-88-3)
• EPA Substance Registry System: 1-Phenyl-3-[(phenylmethyl)amino]-2,5-pyrrolidinedione(7685-88-3)

Safety Data

• Hazardous Substances Data: 7685-88-3(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 100-46-9 benzylamine 

Downstream Products

• 59508-55-3 3-(benzylamino)-1-phenyl-1H-pyrrole-2,5-dione 

Relevant articles and documents

Stereoselective Synthesis of 2-Alkylamino-N-(2'-alhylphenyl)succinimide Conformers

Isolable conformers of 2-alkylamino-N-(2'-alkylphenyl)succinimide were stereoselectively synthesised by amination of N-(2'-alkylphenyl)maleimides.The rotational barrier and the α-methylation of them were investigated.

Cu/Ag-Cocatalyzed Aerobic Oxidative Amination and CuCl2-Mediated Aerobic Oxidative Chloroamination of Maleimides

An efficient Cu(OAc)2/Ag2CO3-cocatalyzed approach for the synthesis of 3-aminomaleimides and 3-amino-4-indolylmaleimides has been developed with satisfactory yields. A series of primary and secondary amines are compatible with this reaction. In addition, treatment of maleimides with primary amines using 1 equiv. of CuCl2leads to the formation of chloroamination products such as 3-amino-4-chloromaleimides by a radical-type mechanism.