128040-48-2

Upstream product

• 50-00-0 formaldehyd 
• 128040-46-0 1-(2-hydroxy-4-methoxyphenyl)-2-(4-fluorophenyl)-1-ethanone 
• 459-22-3 4-fluorophenylacetonitrile 

Downstream Products

• 128040-45-9 4-(2-{4-[3-(4-Fluoro-phenyl)-7-methoxy-2H-chromen-4-yl]-phenoxy}-ethyl)-morpholine 
• 128040-44-8 1-(2-{4-[3-(4-Fluoro-phenyl)-7-methoxy-2H-chromen-4-yl]-phenoxy}-ethyl)-piperidine 
• 125131-76-2 3-(p-fluorophenyl)-7-methoxy-4-chrom-3-ene 
• 128040-42-6 Diethyl-(2-{4-[3-(4-fluoro-phenyl)-7-methoxy-2H-chromen-4-yl]-phenoxy}-ethyl)-amine 

Relevant academic research and scientific papers

A simple one-pot synthesis of isoflavanones

A new simple one-pot synthesis of isoflavanones 2 by reaction of benzyl 2-hydroxyphenylketones 1 with bis(dimethylamino)methane in boiling ethanol is described.

Synthesis of 3-(p-Fluorophenyl)-4-arylchrom-3-enes as Selective Ligands for Antiestrogen-Binding Sites

The synthesis of a series of basic ethers of 3-(p-fluorophenyl)-4-arylchrom-3-enes derived from the isofluoroflavanones is described.Preliminary biological screening shows that most of these compounds were more selective for the antiestrogenbinding sites (AEBS) than the estrogen receptor (ER) in vitro.