1567317-51-4

Basic information

• Product Name: 4-((bis(pyridin-2-ylmethyl)amino)methyl)-N,N-bis(pyridin-2-ylmethyl)aniline
• Synonyms: 4-((bis(pyridin-2-ylmethyl)amino)methyl)-N,N-bis(pyridin-2-ylmethyl)aniline
• CAS NO: 1567317-51-4
• Molecular Weight: 486.619
• Mol File: 1567317-51-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-((bis(pyridin-2-ylmethyl)amino)methyl)-N,N-bis(pyridin-2-ylmethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((bis(pyridin-2-ylmethyl)amino)methyl)-N,N-bis(pyridin-2-ylmethyl)aniline(1567317-51-4)
• EPA Substance Registry System: 4-((bis(pyridin-2-ylmethyl)amino)methyl)-N,N-bis(pyridin-2-ylmethyl)aniline(1567317-51-4)

Safety Data

• Hazardous Substances Data: 1567317-51-4(Hazardous Substances Data)

Upstream product

• 6959-47-3 2-chloromethylpyridine hydrochloride 
• 10003-73-3 4-(aminomethyl)aniline dihydrochloride 

Relevant articles and documents

Synthesis, crystal structure, DNA cleavage properties, and protein binding activities of an unsymmetrical dinuclear copper(II) complex

[Cu2L(phen)(H2O) 3(ClO4)] (ClO4)3 {phen = 1,10-phenanthroline, L = 4-((bis(pyridine2-ylmethyl)amino)methyl)-N,N-bis(pyridin-2-ylmethyl)aniline} was prepared and characterized by physical chemical techniques. The X-ray single-crystal structure analysis shows an unsymmetrical dinuclear species. The interaction of the complex with calfthymus DNA (CT-DNA) was studied by various spectroscopic and viscosity measurements, which indicate that the complex can interact with CT-DNA through intercalation. In the presence of H 2O2, the complex can cleave pBR322 DNA more efficiently and hydroxyl radicals (HO.) may serve as the major cleavage active species. Interactions of the compound with bovine serum albumin (BSA) were also investigated using UV-Vis and fluorescence spectroscopic methods. The results show that the complex quenches the intrinsic fluorescence of BSA by a static quenching mechanism. 2014