131544-72-4

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 14293-14-2 4-(benzyloxy)phenyl benzyl ketone 
• 137070-67-8 1-(4-Benzyloxy-phenyl)-1-(4-methoxy-phenyl)-2-phenyl-ethanol 

Downstream Products

• 131544-89-3 (E)-1,1-dichloro-2-<4-(benzyloxy)phenyl>-2-(4-methoxyphenyl)-3-phenylcyclopropane 

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

Triarylcyclopropanes as antiestrogens and antitumor agents

Triarylcyclopropane derivatives in which one or more of the aryl groups includes a hydroxy as a substituted or unsubstituted or alkoxy or side chain substituent. The compounds are useful as antiestrogens and anti-tumor agents.