70490-63-0

Upstream product

• 6153-06-6 3-methylpent-2-en-4-yn-1-ol 
• 69371-58-0 (E)-1-bromo-3-methylpent-2-en-4-yne 
• 70490-59-4 1-phenylsulfonyl-3-methyl-2-penten-4-yne 
• 100-61-8 N-methylaniline 
• 75168-90-0 1-phenylsulfonyl-4-N-methylphenylamino-3,4-dimethyl-1,3-pentadiene 

Downstream Products

• 83794-50-7 (E)-5-Benzenesulfonyl-3-methyl-pent-3-en-2-one oxime 
• 83794-42-7 N,N'-Bis-[(E)-4-benzenesulfonyl-1,2-dimethyl-but-2-en-(E)-ylidene]-hydrazine 
• 83794-45-0 N-[(E)-4-Benzenesulfonyl-1,2-dimethyl-but-2-en-(E)-ylidene]-N'-phenyl-hydrazine 
• 83794-54-1 Isonicotinic acid [(E)-4-benzenesulfonyl-1,2-dimethyl-but-2-en-(E)-ylidene]-hydrazide 

Relevant academic research and scientific papers

REACTION OF VINYLACETYLENIC SULFONES WITH AROMATIC AMINES

With primary aromatic amines β,γ-unsaturated vinylacetylenic sulfones form azomethine derivatives of α,β-unsaturated ketones.With p-fenylendiamine vinylacetylenic sulfones react to form bisazomethine derivatives of α,β-unsaturated ketones, and with N-methylaniline enamines with the diene fragment in the side chain are formed.The enamines formed in the reaction with secondary aliphatic and aliphatic-aromatic amines are unstable and are rapidly converted into α,β-unsaturated ketones.