94357-76-3

Basic information

• Product Name: 3-(3,4-dimethoxyphenyl)pyrrolidine-2,5-dione
• Synonyms: 3-(3,4-dimethoxyphenyl)pyrrolidine-2,5-dione
• CAS NO: 94357-76-3
• Molecular Weight: 235.24
• Mol File: 94357-76-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(3,4-dimethoxyphenyl)pyrrolidine-2,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,4-dimethoxyphenyl)pyrrolidine-2,5-dione(94357-76-3)
• EPA Substance Registry System: 3-(3,4-dimethoxyphenyl)pyrrolidine-2,5-dione(94357-76-3)

Safety Data

• Hazardous Substances Data: 94357-76-3(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 2286-55-7 ethyl α-cyano-β-(3,4-dimethoxyphenyl)acrylate 
• 6286-49-3 2-(3,4-dimethoxyphenyl)succinonitrile 
• 38175-28-9 (3,4-dimethoxy-phenyl)-succinic acid-anhydride 

Downstream Products

• 94357-77-4 2-(3,4-dimethoxyphenyl)-N-(n-propyl)succinimide 
• 120238-23-5 3-(3,4-dimethoxyphenyl)-4-ethoxalyl-1-(methyl)pyrrolidine-2,5-dione 
• 120238-25-7 3-(3,4-dimethoxyphenyl)-1-methyl-4-(methylene)pyrrolidine-2,5-dione 
• 120238-28-0 3-(3,4-dimethoxyphenyl)-1,4-dimethyl-3-pyrroline-2,5-dione 
• 143883-93-6 (3R,4R)-1-Butyl-3-(3,4-dimethoxy-phenyl)-4-methyl-pyrrolidine 
• 143883-86-7 3-(3,4-Dimethoxy-phenyl)-1-pentyl-pyrrolidine 
• 143883-77-6 3-(3,4-Dimethoxy-phenyl)-1-isopropyl-pyrrolidine 
• 144076-30-2 3-(3,4-dihydroxy)phenyl-1-(n-hexyl)pyrrolidine hydrobromide 
• 144076-32-4 4-((3R,4R)-1-Butyl-4-methyl-pyrrolidin-3-yl)-benzene-1,2-diol; hydrobromide 
• 144076-29-9 4-(1-Pentyl-pyrrolidin-3-yl)-benzene-1,2-diol; hydrobromide 
• 144076-26-6 4-(1-Butyl-pyrrolidin-3-yl)-benzene-1,2-diol; hydrobromide 
• 144076-25-5 4-(1-Isopropyl-pyrrolidin-3-yl)-benzene-1,2-diol; hydrobromide 
• 143883-92-5 cis-1-(n-butyl)-3-(3,4-dihydroxyphenyl)-4-(methyl)pyrrolidine-2,5-dione 
• 143883-89-0 3-(3,4-Dimethoxy-phenyl)-1-hexyl-pyrrolidine 

Relevant articles and documents

Synthesis and dopaminergic activity of 3-(3,4-dihydroxyphenyl)-1-n-propylpyrrolidine hydrobromide

3-(3,4-Dihydroxyphenyl)-1-n-propylpyrrolidine hydrobromide was synthesized by a six-step reaction sequence and was evaluated, and compared with apomarphine, for central dopaminergic agonist activity. The compound produced behavioral and biochemical change