162011-52-1

Upstream product

• 490-78-8 2,5-Dihydroxyacetophenone 
• 402-23-3 1-bromomethyl-3-trifluoromethylbenzene 

Downstream Products

• 162011-57-6 1-[2-((S)-1-Oxiranylmethoxy)-5-(3-trifluoromethyl-benzyloxy)-phenyl]-ethanone 
• 162118-77-6 1-[2-((S)-2-Hydroxy-3-methoxy-propoxy)-5-(3-trifluoromethyl-benzyloxy)-phenyl]-ethanone 
• 162118-79-8 1-[2-((R)-2-Hydroxy-3-methoxy-propoxy)-5-(3-trifluoromethyl-benzyloxy)-phenyl]-ethanone 

Relevant academic research and scientific papers

Alkylbenzyl ethers of hydroquinones as monoamine oxidase B inhibitors

A series of alkylbenzylethers of substituted hydroquinone analogs of 4-(3-chlorophenyl methyloxy)-phenoxybutyronitrile I, and alcohol II were synthesized as monoamine oxidase (MAO) inhibitors. Incorporation of electron-withdrawing groups on the hydroquinone afforded compounds with higher levels of activity and selectivity than I or II for MAO B inhibition.