85277-72-1

Upstream product

• 33155-61-2 tert-butyl 2-(4-methoxyphenyl)acetate 
• 75-45-6 Chlorodifluoromethane 
• 85277-61-8 1-tert-butyl 3-ethyl 2-(4-methoxyphenyl)malonate 

Downstream Products

• 85277-94-7 (E)-3-fluoro-2-(4-methoxyphenyl)prop-2-en-1-ol 
• 85277-85-6 (E)-ethyl 3-fluoro-2-(4-methoxyphenyl)acrylate 
• 85278-03-1 (E)-1-Fluoro-2-(4'-methoxy)phenyl-3-phthalimidopropene 
• 85278-11-1 (E)-3-Fluoro-2-(4-methoxy-phenyl)-allylamine; hydrochloride 

Relevant academic research and scientific papers

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