87293-06-9

Upstream product

• 74211-55-5 2-(4-Methylphenyl)-3-chlor-N-phenyl-maleinimid 
• 3152-16-7 1-(4-Methylphenyl)maleinsaeureanhydrid 
• 87292-74-8 1-(4-Methylphenyl)-2-chlor-maleinsaeureanhydrid 

Downstream Products

• 87293-01-4 2-(4-Methylphenyl)-3-amino-N-phenyl-maleinimid 
• 76039-44-6 6-Methyl-2-phenyl-4H-pyrrolo[3,4-b]indole-1,3-dione 
• 87293-03-6 2-(4-Methylphenyl)-3-triphenylphosphanimino-N-phenyl-maleinimid 
• 76039-48-0 6-Methyl-2-(morpholine-4-carbonyl)-1H-indole-3-carboxylic acid phenylamide 
• 76039-45-7 6-Methyl-1H-indole-2,3-dicarboxylic acid 2-cyclohexylamide 3-phenylamide 
• 76039-49-1 6-Methyl-1H-indole-2,3-dicarboxylic acid 2-benzylamide 3-phenylamide 
• 76039-50-4 6-Methyl-1H-indole-2,3-dicarboxylic acid bis-phenylamide 
• 76039-42-4 6-Methyl-3-phenylcarbamoyl-1H-indole-2-carboxylic acid ethyl ester 
• 76039-41-3 6-Methyl-3-phenylcarbamoyl-1H-indole-2-carboxylic acid methyl ester 
• 76039-47-9 6-Methyl-3-phenylcarbamoyl-1H-indole-2-carboxylic acid 

Relevant academic research and scientific papers

Synthesis and Reaction Behaviour of 2-Aryl-3-chloro-maleimides

2-Aryl-3-chloro-maleimides 2 are prepared by the chlorination of aryl-maleicanhydrides and aminolysis of the resulting 1-aryl-2-chloro-maleicanhydrides 1.The imide 2a is reacted with N-, S-, O- and C-nucleophiles and inorganic salts to give 2,3-disubstitu

SYNTHESE VON CHINOXALIN- UND INDOL-2,3-DICARBONSAUREIMIDEN

Quinoxaline- and indole-2,3-dicarboxylic imides 7,8 are prepared by reaction of halogenactive maleimides 1,2 with sodium azide.Further derivatives of these heterocyclic series are available by secondary reactions of the imides.