1057516-18-3

Upstream product

• 515159-59-8 3,4,4-trichloro-1-(4-methylphenyl)-3-buten-1-one 

Downstream Products

• 1057516-25-2 (E)-2-bromo-4,4-dichloro-1-(4-methylphenyl)-3-morpholinobut-2-en-1-one 
• 1057516-37-6 4-methoxy-5-(4-methylbenzoyl)-1H-pyrazole 
• 1057516-45-6 4-methoxy-3-(4-methylphenyl)isoxazole-5-carbaldehyde oxime 
• 93-58-3 benzoic acid methyl ester 
• 100-47-0 benzonitrile 
• 1057516-53-6 4-(4-methylphenyl)-5-trichlorovinyl-1,3-thiazol-2-amine 
• 1057516-61-6 N-[4-(4-methylphenyl)-5-trichlorovinyl-1,3-thiazol-2-yl]acetamide 

Relevant academic research and scientific papers

Synthesis of 3,4-dibromo-3,4,4-trichloro-1-phenylbutan-1-one and 1-aryl-2-bromo-3,4,4-trichlorobut-3-en-1-ones from 3,4,4-trichlorobut-3-enoic acid

Bromination of 3,4,4-trichlorobut-3-enoic acid in boiling carbon tetrachloride led to the formation of 2-bromo-3,4,4-trichlorobut-3-enoic acid as a result of replacement of hydrogen in the CH2 group. The reaction at 40°C involved the double C=C