13278-76-7

Upstream product

• 589-10-6 phenoxyethyl bromide 
• 100-09-4 4-methoxybenzoic acid 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 87261-94-7 1-<4-(2-bromoethoxy)phenyl>-1-(4-methoxyphenyl)-2-phenylethene 
• 30170-81-1 1-[4-(2-Bromo-ethoxy)-phenyl]-1-(4-methoxy-phenyl)-2-phenyl-ethanol 
• 95393-33-2 2-phenoxy>-N-ethylpyrrolidin-2-one 
• 87261-95-8 2-phenoxy>-N-ethylpyrrolidin-2-one 
• 87261-94-7 (Z/E)-1-<4-(2-bromoethoxy)phenyl>-1-(4-methoxyphenyl)-2-phenyl ethene 
• 131544-86-0 (Z)-1,1-dichloro-2-<4-<2-(dimethylamino)ethoxy>phenyl>-2-(4-methoxyphenyl)-3-phenylcyclopropane 

Relevant academic research and scientific papers

Preparation of prodrugs for selective drug delivery

Synthesis of a chemical compound having the formula A-B-C that may serve for applications such as drug delivery where A is a chemiluminescent, moiety, B is a photochromic moiety, and C is a biologically active moiety where A-B-C may serve as a prodrug. No

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