131544-89-3

Upstream product

• 67-66-3 chloroform 
• 131544-73-5 Z-1-(4-benzyloxyphenyl)-1-(4-methoxyphenyl)-2-phenyl ethene 
• 131544-72-4 1-(4-Benzyloxyphenyl)-1-(4-methoxyphenyl)-2-phenylethene 
• 14293-14-2 4-(benzyloxy)phenyl benzyl ketone 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 137070-67-8 1-(4-Benzyloxy-phenyl)-1-(4-methoxy-phenyl)-2-phenyl-ethanol 

Downstream Products

• 131544-85-9 (E)-1,1-dichloro-2-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-3-phenylcyclopropane 
• 131544-86-0 (Z)-1,1-dichloro-2-<4-<2-(dimethylamino)ethoxy>phenyl>-2-(4-methoxyphenyl)-3-phenylcyclopropane 
• 131544-85-9 (E)-1,1-dichloro-2-(4-hydroxyphenyl)-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

Synthesis and Biological Evaluation of a Series of 1,1-Dichloro-2,2,3-triarylcyclopropanes as Pure Antiestrogens

A series of 1,1,-dichloro-2,2,3-triarylcyclopropanes (DTACs) was synthesized and evaluated as pure antiestrogens.Addition of 4-methoxy- or 4-(benzyloxy)phenyl Grignard reagents to p-methoxy, p-benzyloxy, or unsubstituted deoxybenzoins, followed by dehydra