887580-87-2

Upstream product

• 767-00-0 4-cyanophenol 
• 29147-90-8 4-decyloxybenzonitrile 
• 2050-77-3 Iododecane 
• 112-29-8 1-bromo dodecane 

Downstream Products

• 1589489-88-2 N,N'-bis(4-decyloxybenzyl)naphthalene-2,6-diamine 
• 1589489-89-3 3-(2-methoxynaphthalene-1-yl)propynoic acid N-{[4-(decyloxy)phenyl]methyl}-N-[6-(N-{[4-(decyloxy)phenyl]methyl}-3-(2-methoxynaphthalen-1-yl)prop-2-ynamido)naphthalen-2-yl]amide 
• 1040198-10-4 [Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2]⁽¹⁺⁾*BF₄^(1-)=[Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2][BF₄] 
• 1040198-03-5 [Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2]⁽¹⁺⁾*NO₃^(1-)=[Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2][NO₃] 
• 1040198-14-8 [Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2]⁽¹⁺⁾*CH₃COO^(1-)=[Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2][CH₃COO] 
• 1040198-25-1 [Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2]⁽¹⁺⁾*CF₃SO₃^(1-)=[Ag(NH₂CH₂C₆H₄OC₁₀H₂₁)2][CF₃SO₃] 

Relevant academic research and scientific papers

AMINE COMPOUNDS HAVING ANTI-INFLAMMATORY, ANTIFUNGAL, ANTIPARASITIC AND ANTICANCER ACTIVITY

Amine compounds having activity against inflammation, fungi, unicellular parasitic microorganisms, and cancer are described. The compounds contain a monocyclic, bicyclic, or tricyclic aromatic ring having one, two, or three ring nitrogen atoms.

Enantioselective synthesis and enhanced circularly polarized luminescence of S-shaped double azahelicenes

The enantioselective synthesis of azahelicenes and S-shaped double azahelicenes has been achieved via the Au-catalyzed sequential intramolecular hydroarylation of alkynes. The use of excess AgOTf toward a Au(I) complex is crucial for this transformation. Interestingly, the circularly polarized luminescence activity of the S-shaped double azahelicenes was significantly higher than that of the azahelicenes.