78486-52-9

Upstream product

• 83583-95-3 1-N-(p-chlorobenzoyl)-p-methylphenylamino-3-(p-methylphenylimino)-1-butene 
• 83583-97-5 1--3-(p-methylphenylimino)-1-butene 
• 78486-47-2 1-(N-benzoyl-p-methylphenylamino)-3-(p-methylphenylimino)-1-butene 
• 78486-46-1 1-(N-benzoyl-p-methylphenyloamino)-3-(p-methylphenylimino)-1-propene 
• 78486-51-8 1,3-bis(N-benzoyl-p-toluidino)-1,3-butadiene 

Downstream Products

• 83583-97-5 1--3-(p-methylphenylimino)-1-butene 
• 106237-26-7 β-(p-methylphenylamino)crotonaldehyde 
• 83583-98-6 1,3-bis-1,3-butadiene 
• 83583-96-4 1,3-bis-1,3-butadiene 
• 106237-32-5 3--1-(p-methylphenylimino)-2-butene 
• 106256-68-2 4-Chloro-N-((E)-1-methyl-3-oxo-propenyl)-N-p-tolyl-benzamide 
• 83583-91-9 1-(N-acetyl-p-methylphenylamino)-3-(p-methylphenylimino)-1-propene 
• 83583-92-0 1,3-bis(N-acetyl-p-toluidino)-1,3-butadiene 
• 83583-95-3 1-N-(p-chlorobenzoyl)-p-methylphenylamino-3-(p-methylphenylimino)-1-butene 

Relevant academic research and scientific papers

Hydrolysis of Acyl Derivatives of Malonaldehyde Dianil. IV. Preparation of β-(p-Toluidino)crotonaldehyde

β-(p-Toluidino)crotonaldehyde (V), a possible reactant of the Combes reaction, was prepared by the alkaline hydrolysis of β-N-(p-chlorobenzoyl)-p-toluidinocrotonaldehyde (XXIV).Compound XXIV was prepared by the hydrochloric acid-catalyzed hydrolysis of 3-