85278-33-7

Upstream product

• 85278-32-6 ethyl 2-phenyl-3,3-difluoroacrylate 
• 85278-30-4 ethyl 2-(tert-butoxycarbonyl)-2-(bromodifluoromethyl)phenylacetate 
• 85277-62-9 ethyl 2-(tert-butoxycarbonyl)phenylacetate 

Downstream Products

• 85278-35-9 1,1-difluoro-2-phenyl-3-phthalimidopropene 
• 85278-37-1 (3,3-Difluoro-2-phenyl-allyl)-carbamic acid tert-butyl ester 
• 85278-38-2 3,3-difluoro-2-phenylprop-2-en-1-aminium chloride 
• 85278-36-0 2-phenyl-3,3-difluoroallylamine 

Relevant academic research and scientific papers

Inactivation of bovine plasma amine oxidase by haloallylamines

Various 2- and 3-haloallylamines were synthesized and evaluated as inhibitors of the quinone-dependent bovine plasma amine oxidase (BPAO). 3-Haloallylamines, which were previously found to be good inhibitors of the flavin-dependent mitochondrial monoamine

Facile Syntheses of gem-Difluoroalkenes from Chlorodifluoromethylketones

Chlorodifluoromethyl ketones reacted with diazomethane to afford epoxides in high yield; upon treatment with butyllithium, the epoxides underwent efficient ring opening to afford 3,3-difluoro-2-alkyl-alken-1-ols, suitable substrates for sigmatropic rearra

Enzyme-activated irreversible inhibitors of monoamine oxidase: Phenylallylamine structure-activity relationships

Seventeen 2-aryl-3-haloallylamine derivatives were prepared and evaluated as inhibitors of monoamine oxidase (MAO, EC 1.4.3.4). The synthesis of these compounds was achieved from either α-methylstyrene or ring-substituted phenylacetic acid derivatives. Wi

Allyl amine MAO inhibitors

Compounds of the formula STR1 wherein: R is phenyl, phenyl monosubstituted, disubstituted, or trisubstituted by (C1 -C8) alkyl, (C1 -C8)alkoxy, hydroxy, chlorine, bromine, iodine, fluorine, trifluoromethyl, nitr