40891-23-4

Upstream product

• 60-35-5 acetamide 
• 72721-58-5 2-acetylamino-2-morpholin-4-yl-1-phenyl-ethanone 
• 6425-12-3 1-phenyl-2,2-dimorpholin-1-yl-ethanone 
• 1074-12-0 phenylglyoxal hydrate 

Downstream Products

• 72721-82-5 N-[1-Acetylamino-2-(4-bromo-phenyl)-2-phenyl-ethyl]-acetamide 
• 72721-81-4 N-[1-Acetylamino-2-(4-chloro-phenyl)-2-phenyl-ethyl]-acetamide 
• 72721-80-3 N-(1-Acetylamino-2-phenyl-2-p-tolyl-ethyl)-acetamide 
• 72721-79-0 Bis(1,1-acetylamino)-2,2-diphenylaethan 
• 28523-15-1 2-(4-chlorophenyl)-2-phenylacetaldehyde 
• 16343-34-3 2-(4-bromophenyl)-2-phenylethanal 
• 32556-48-2 N-(2-methyl-5-phenyl-oxazol-4-yl)-acetamide 
• 72721-75-6 Bis(1,1-acetylamino)-2-hydroxy-2-phenylaethan 

Relevant academic research and scientific papers

Removal of Toluene-p-sulphonyl Groups from Sulphonamides. Part 4. Synthesis of Phenylglyoxal Imine Monomers

Syntheses and reactions of N-tosylphenacylamines with bases have been systematically examined.Monomeric C-methoxy-imines are available from some of these reactions.C-Methoxyphenacylarylamines, made by two routes, were converted into monomeric imines on treatment with noble-metal catalysts, The boron trifluoride-catalysed reactions of aryl aldehydes with sulphonamides provide a new and convenient route to N-sulphonylarylimines.