69584-78-7

Upstream product

• 4548-45-2 2-chloro-5-nitropyridine 
• 86-29-3 Diphenylacetonitrile 

Downstream Products

• 1042365-22-9 6-benzhydryl-piperidin-3-ylamine 
• 374562-17-1 2-(5-aminopyridin-2-yl)-2,2-diphenylacetamide 
• 374562-19-3 6-benzhydrylpyridin-3-ylamine 
• 374562-15-9 2-(5-nitropyridin-2-yl)-2,2-diphenylacetamide 

Relevant academic research and scientific papers

Interaction of cis-(6-benzhydrylpiperidin-3-yl)benzylamine analogues with monoamine transporters: Structure-activity relationship study of structurally constrained 3,6-disubstituted piperidine analogues of (2,2-diphenylethyl)-[1-(4-fluorobenzyl)piperidin-

To explore structure-activity relationships (SAR) of a novel conformationally constrained lead cis-3,6-disubstituted piperidine derivative derived from (2,2-diphenylethyl)-[1-(4-fluorobenzyl)-piperidine-4-ylmethyl]amine (I), a series of compounds was synt

N-and o-substituted 4-[2-( diphenylmethoxy) -ethyl]-1- (phenyl) methyl) piperidine analogs and methods of treating cns disorders therewith

N- and O-substituted 4[2-diaromaticmethoxy and methylamino)alkyl]piperidines exhibit high CNS activity with respect to the dopamine transporter (DAT) and serotonin transporter (SERT). Preferred compounds exhibit highly differential behavior as between the

Rational design and synthesis of novel 2,5-disubstituted cis- and trans-piperidine derivatives exhibiting differential activity for the dopamine transporter

Herein, we report the rational design and synthesis of novel 2,5-disubstituted piperidine derivatives in the cis and trans isomeric forms. Out of these two isomers, the cis-isomer, 7a, was found to exhibit the most potent activity and selectivity for the