87261-94-7

Upstream product

• 13278-76-7 4-(2-bromoethoxy)-4'-methoxybenzophenone 
• 100-44-7 benzyl chloride 
• 100-09-4 4-methoxybenzoic acid 
• 589-10-6 phenoxyethyl bromide 
• 30170-81-1 1-[4-(2-Bromo-ethoxy)-phenyl]-1-(4-methoxy-phenyl)-2-phenyl-ethanol 

Downstream Products

• 87261-95-8 2-phenoxy>-N-ethylpyrrolidin-2-one 
• 131544-86-0 (Z)-1,1-dichloro-2-<4-<2-(dimethylamino)ethoxy>phenyl>-2-(4-methoxyphenyl)-3-phenylcyclopropane 
• 95393-33-2 2-phenoxy>-N-ethylpyrrolidin-2-one 

Relevant academic research and scientific papers

Synthesis and chiral separation of some antitumor agents

Four Z-isomers of 1,1-dichloro-2,2,3-triarylcyclopropane (DTACs), designed as potent antitumor agents, were synthesized from their appropriately substituted ethenes, which were prepared from the Grignard reaction followed by the dehydration of their inter

Estrogen Receptor Binding and Estrogenic/Antiestrogenic Effects of Two New Metabolites of Nitromiphene, 2-phenoxy>-N-ethylpyrrolidine

Reduction of the triarylethylene antiestrogen 2--N-ethylpyrrolidine (1) with sodium borohydride-stannous chloride afforded 2-(p-methoxyphenyl)-p'-(2-pyrrolidin-1-yl-ethoxy)deoxybenzoin (2).Incubation of