115462-46-9

Upstream product

• 115462-38-9 2-(3-Methylphenoxy)-1-(2-pyridyl)ethanol 
• 100-69-6 2-vinylpyridine 
• 55967-94-7 2-oxiranylpyridine 
• 115462-64-1 1-[2-(1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 
• 115462-46-9 1-Piperidin-2-yl-2-m-tolyloxy-ethanol 
• 108-39-4 3-methyl-phenol 
• 115462-64-1 1-[2-(1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 
• 115462-64-1 1-[(R)-2-((R)-1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 

Downstream Products

• 115462-47-0 (R)-1-(S)-Piperidin-2-yl-2-m-tolyloxy-ethanol 
• 115462-46-9 1-Piperidin-2-yl-2-m-tolyloxy-ethanol 
• 115462-46-9 1-Piperidin-2-yl-2-m-tolyloxy-ethanol 
• 115462-64-1 1-[2-(1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 
• 115462-65-2 1-[(R)-2-((S)-1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 
• 115462-64-1 1-[(R)-2-((R)-1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 
• 115462-64-1 1-[2-(1-Hydroxy-2-m-tolyloxy-ethyl)-piperidin-1-yl]-ethanone 

Relevant academic research and scientific papers

Synthesis of 2-aryloxy- and 2-arylalkoxy-1-(2-piperidyl)ethanols

The preparation and separation of diastereomeric pairs of a series of 2-aryloxy- and 2-arylalkoxy-1-(2-piperidyl)ethanols is reported. The erythro aminoalcohols were converted into threo isomers by thionyl chloride treatment of their N-acetyl derivatives

Synthesis and β-adrenergic antagonism of 2-(aryloxy)-1-(2-piperidyl)ethanols

A series of erythro- and threo-2-(aryloxy)-1-(2-piperidyl)ethanol derivatives (3) was synthesized from 2-(2-oxiranyl)pyridine for evaluation as β-antagonists. Most compounds displayed high competitive β-blocking potency, but they lacked significant β