133534-69-7

Upstream product

• 94-71-3 2-Ethoxyphenol 
• 133534-59-5 (RS,RS) 2-hydroxy-3-(2-ethoxyphenoxy)-3-benzenepropanoic acid 
• 133534-56-2 (RS,RS) methyl 2-hydroxy-3-(2-ethoxyphenoxy)-3-benzenepropanoate 
• 19190-78-4 potassium trans-3-phenyloxiranecarboxylate 
• 133534-59-5 (RS,SR) 2-hydroxy-3-(2-ethoxyphenoxy)-3-benzenepropanoic acid 
• 133534-56-2 (RS,SR) methyl 2-hydroxy-3-(2-ethoxyphenoxy)-3-benzenepropanoate 
• 19190-78-4 potassium cis-3-phenyloxiranecarboxylate 

Downstream Products

• 133534-75-5 (RS,SR) ethyl<(1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl)ethyl>imidoate hydrochloride 
• 133534-38-0 (RS,RS) 1-ethyl-2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-1H-imidazole 
• 133534-34-6 (RS,RS) 1-ethyl-2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-4,5-dihydro-1H-imidazole 
• 133534-32-4 (RS,RS) 2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-4,5-dihydro-1H-imidazole 
• 133534-36-8 (RS,RS) 2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-1H-imidazole 
• 133534-63-1 (RS,RS) 2-methoxy-3-(2-ethoxyphenoxy)-benzenepropanenitrile 
• 133534-75-5 (RS,RS) ethyl<(1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl)ethyl>imidoate hydrochloride 
• 133534-38-0 (RS,SR) 1-ethyl-2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-1H-imidazole 
• 133534-34-6 (RS,SR) 1-ethyl-2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-4,5-dihydro-1H-imidazole 
• 133534-36-8 (RS,SR) 2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-1H-imidazole 
• 133534-48-2 (RS,SR) 2-<1-methoxy-2-(2-ethoxyphenoxy)-2-phenyl>ethyl-4,5-dihydro-1H-imidazole hydrochloride 
• 133534-63-1 (RS,SR) 2-methoxy-3-(2-ethoxyphenoxy)-benzenepropanenitrile 

Relevant academic research and scientific papers

Research of potential antidepressant drugs with α2-adrenoreceptor antagonist and NA-uptake inhibiting properties: synthesis of 2-(1-hydroxy-2-phenoxy-2-phenyl)ethyl-4,5-dihydro-1H-imidazole derivatives

A series of 2-(1-hydroxy-2-phenoxy-2-phenyl)ethyl-4,5-dihydro-1H-imidazole derivatives has been synthesized with the aim of finding potential antidepressant drugs endowed with both NA-uptake and α2-antagonist properties.The structure of the new