267409-96-1

Upstream product

• 5807-30-7 3,4-dichlorophenyl acetic acid 
• 106-95-6 allyl bromide 

Downstream Products

• 910028-58-9 (1R,5S)-1-(3,4-dichlorophenyl)-3-oxabicyclo[3.1.0]hexan-2-one 
• 846060-58-0 (-)-1-(3,4-dichlorophenyl)-3-oxa-bicyclo[3.1.0]hexan-2-one 
• 1280479-73-3 C₂₉H₃₇Cl₂FN₄O₂ 
• 1280479-74-4 C₂₉H₃₅Cl₂FN₄O₂ 
• 1280479-75-5 C₂₈H₃₅Cl₂FN₄O₂ 
• 1280479-77-7 C₃₀H₃₇Cl₂FN₄O₂ 
• 1280479-79-9 C₂₉H₃₅Cl₂FN₄O₂ 
• 1280479-82-4 C₂₅H₃₁Cl₂FN₄O₃S 
• 1280479-83-5 C₂₇H₃₃Cl₂FN₄O₃S 
• 1280479-85-7 C₃₁H₃₉Cl₂FN₄O₂ 
• 1280479-87-9 C₂₈H₃₆Cl₂FN₅O₃S 
• 1280478-83-2 (1S,2R)-1-(3,4-dichlorophenyl)-2-hydroxymethylcyclopropanecarboxylic acid benzyl methyl amide 
• 846060-70-6 (1S,2R)-1-(3,4-dichlorophenyl)-2-hydroxymethylcyclopropanecarboxylic acid (4-fluorobenzyl)methylamide 

Relevant academic research and scientific papers

Studies on the structure-activity relationship of bicifadine analogs as monoamine transporter inhibitors

Compounds with various activities and selectivities were discovered through structure-activity relationship studies of bicifadine analogs as monoamine transporter inhibitors. The norepinephrine-selective 2-thienyl compound S-6j was efficacious in a rodent