128643-13-0

Upstream product

• 42876-07-3 2-(2-aminophenoxy)ethan-1-ol 
• 75-36-5 acetyl chloride 
• 16365-25-6 2-(2-hydroxyethoxy)nitrobenzene 
• 88-75-5 2-hydroxynitrobenzene 
• 148-24-3 8-quinolinol 
• 614-76-6 N-acetyl-2-bromoaniline 

Downstream Products

• 850895-67-9 2-(2-acetylaminophenoxy)-1-mesyloxyethane 
• 688307-35-9 2-(2-acetylaminophenoxy)ethylamine 
• 850895-68-0 2-(2-acetylaminophenoxy)-1-dibenzylaminoethane 
• 850896-15-0 (2S)-2-[((2-(2-acetylaminophenoxy)ethyl)-amino)methyl]-1,4-benzodioxane 

Relevant academic research and scientific papers

QSAR study for a novel series of ortho monosubstituted phenoxy analogues of α1-adrenoceptor antagonist WB4101

A number of (S)- and (R)-2-[(2-phenoxyethyl)aminomethyl]-1,4-benzodioxanes unsubstituted or ortho monosubstituted at the phenoxy moiety were synthesized and tested in binding assays on the α1a-AR, α1b-AR, α1d-AR and the 5-

Process for producing alkoxybenzene compound and aryloxybenzene compound

The present invention relates to a process for producing an alkoxybenzene compound or an aryloxybenzene compound by reacting a halogenobenzene compound with an alcohol or a phenol compound in the presence of copper or a copper compound, an amine, and a base. According to the disclosure, an alkoxybenzene compound and an aryloxybenzene compound can be produced under moderate conditions in good yield with high selectivity.