66504-57-2

Upstream product

• 930-88-1 N-methylmaleimide 
• 19183-05-2 3-methoxy-benzenediazonium; chloride 
• 536-90-3 m-Anisidine 
• 1159989-34-0 C₁₂H₁₂ClNO₃ 

Downstream Products

• 88905-19-5 4,4-dimethoxy-1-(3-methoxyphenyl)-N-methyl-1,2-cyclobutanedicarboximide 
• 88905-28-6 bis(3-methoxyphenyl)-N,N'-dimethyl-1,2,3,4-cyclobutane-tetracarboxylic 1,2:3,4-diimide 
• 88905-27-5 6,6-dimethoxy-5-(3-hydroxyphenyl)-3-methyl-3-azabicyclo<3.2.0>heptane 
• 88905-29-7 5-(3-methoxyphenyl)-3-azabicyclo<3.2.0>heptan-6-one 
• 88905-23-1 6,6-dimethoxy-5-(3-methoxyphenyl)-3-methyl-3-azabicyclo<3.2.0>heptane 
• 88905-30-0 5-(3-methoxyphenyl)-3,5',5'-trimethylspiro<3-azabicyclo<3.2.0>heptane-6,2'-<1,3>dioxane> 

Relevant academic research and scientific papers

Inhibition of monoamine oxidase B by N-methyl-2-phenylmaleimides

Based on a recent report that 1-methyl-3-phenylpyrrolyl analogues are moderately potent reversible inhibitors of the enzyme monoamine oxidase B (MAO-B), a series of structurally related N-methyl-2-phenylmaleimidyl analogues has been prepared and evaluated

3a-(substituted phenyl)-2,3,3a,4,7,7a-hexahydro[or 3a-(substituted-phenyl)octahydro]-4,7-alkano-1H-isoindoles for treating depression in warm-blooded animals

This disclosure describes 3a-(substituted-phenyl)-2,3,3a,4,7,7a-hexahydro[or 3a-(substituted-phenyl)octahydro]-4,7-alkano-1H-isoindoles which possess activity as antidepressants and as antistress agents in mammals.

5-Aryl-3-azabicycloheptan-6-one Ketals, Compounds with Morphine-Like Analgesic Activity

A series of 5-aryl-3-azabicycloheptan-6-one ketals 6 were synthesized by hydride reduction of 1-aryl-4,4-dimethoxy-1,2-cyclobutanedicarboximides 5.Imides 5 were obtained as the sole, regioselective products of the photocycloaddition of 1,1-

Diels-Alder Dimerization of 2-Arylmaleimides. X-Ray Crystal Structure of the Dimer of 2-p-Tolylmaleimide

Dimers (4) and (7) were obtained during the course of the Meerwein arylation reaction; a Diels-Alder reaction is proposed for the mechanism of the dimerization, and the X-ray structure of (4) is reported.