124398-01-2

Upstream product

• 107-13-1 acrylonitrile 
• 6407-35-8 N-cyclohexylidenemethylamine 

Downstream Products

• 124398-08-9 N-methyl-N-<6-(β-cyanoethyl)-1-cyclohexenyl>dichloroacetamide 
• 124409-21-8 N-[6-(2-Cyano-ethyl)-cyclohex-1-enyl]-N-methyl-benzamide 
• 124398-04-5 4-Chloro-N-[6-(2-cyano-ethyl)-cyclohex-1-enyl]-N-methyl-benzamide 
• 124398-02-3 N-[6-(2-Cyano-ethyl)-cyclohex-1-enyl]-4-methoxy-N-methyl-benzamide 
• 103582-18-9 N-methyl-N-<2-(β-cyanoethyl)-2-cyclohexenyl>acetamide 
• 103582-17-8 N-methyl-N-<2-(β-cyanoethyl)-6-cyclohexenyl>acetamide 
• 124398-07-8 N-methyl-N-<6-(β-cyanoethyl)-1-cyclohexenyl>monochloroacetamide 
• 124398-09-0 2,2,2-Trichloro-N-[6-(2-cyano-ethyl)-cyclohex-1-enyl]-N-methyl-acetamide 
• 124398-06-7 N-methyl-N-<6-(β-cyanoethyl)-1-cyclohexenyl>-3-nitrobenzamide 
• 124398-10-3 N-methyl-N-<6-(β-cyanoethyl)-1-cyclohexenyl>trifluoroacetamide 
• 124398-05-6 4-Bromo-N-[6-(2-cyano-ethyl)-cyclohex-1-enyl]-N-methyl-benzamide 
• 124398-03-4 N-methyl-N-<6-(β-cyanoethyl)-1-cyclohexenyl>-4-methylbenzamide 

Relevant academic research and scientific papers

ISOMERISM AND STRUCTURE OF THE PRODUCT FROM THE N-ACETYLATION OF N-METHYL-2-(-β-CYANOETHYL)CYCLOHEXANONE IMINE

The product from the N-acetylation of N-methyl-2-(β-cyanoethyl)cyclohexanone imine was isolated as a mixture of the isomeric enamine forms with a trisubstitute (A) and tetrasubstituted (B) C=C double bond.The equilibrium between forms A and B was investig