85277-65-2

Upstream product

• 33155-59-8 tert-butyl 2-(4-chlorophenyl)acetate 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 85278-08-6 (E)-2-(4-Chloro-phenyl)-3-fluoro-allylamine; hydrochloride 
• 85278-00-8 (E)-1-Fluoro-2-(4'-chloro)phenyl-3-phthalimidopropene 
• 85277-82-3 ethyl (E)-2-(4-chlorophenyl)-3-fluoroacrylate 
• 85277-91-4 (E)-2-(4-Chloro-phenyl)-3-fluoro-prop-2-en-1-ol 
• 85277-74-3 Ethyl 2-difluoromethyl-2-carbo-tert-butoxy(4'-chloro)phenylacetate 

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