1589489-88-2

Basic information

• Product Name: N,N'-bis(4-decyloxybenzyl)naphthalene-2,6-diamine
• Synonyms: N,N'-bis(4-decyloxybenzyl)naphthalene-2,6-diamine
• CAS NO: 1589489-88-2
• Molecular Weight: 650.988
• Mol File: 1589489-88-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N'-bis(4-decyloxybenzyl)naphthalene-2,6-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-bis(4-decyloxybenzyl)naphthalene-2,6-diamine(1589489-88-2)
• EPA Substance Registry System: N,N'-bis(4-decyloxybenzyl)naphthalene-2,6-diamine(1589489-88-2)

Safety Data

• Hazardous Substances Data: 1589489-88-2(Hazardous Substances Data)

Upstream product

• 887580-87-2 [4-(decyloxy)phenyl]methanamine 
• 13720-06-4 2,6-dibromonaphthalene 
• 2050-77-3 Iododecane 
• 29147-90-8 4-decyloxybenzonitrile 
• 767-00-0 4-cyanophenol 

Downstream Products

• 1589489-81-5 C₈₈H₈₆N₂O₆ 
• 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 

Relevant articles and documents

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.