15395-61-6

Basic information

• Product Name: 2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine
• CAS NO: 15395-61-6
• Molecular Formula: C₁₃H₁₅N₃
• Molecular Weight: 213.2783
• Mol File: 15395-61-6.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 346.5°C at 760 mmHg
• Flash Point: 163.4°C
• Density: 1.095g/cm³
• Vapor Pressure: 5.72E-05mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: 2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine(15395-61-6)
• EPA Substance Registry System: 2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine(15395-61-6)

Safety Data

• Hazardous Substances Data: 15395-61-6(Hazardous Substances Data)

Usage

General Description

2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine, also known as 2-(2-pyridyl)ethylamine, is a chemical compound with the molecular formula C12H14N2. It is a member of the amine class of compounds and contains two pyridine rings in its structure. 2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine is commonly used in organic synthesis and chemical research as a building block for creating more complex molecules. It is important for the pharmaceutical industry as it can be used in the creation of new drugs and medications. Additionally, 2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)ethanamine is known for its potential biological activity and may have applications as a pharmacological agent.

Upstream product

• 2706-56-1 2-(aminoethyl)pyridine 
• 6959-47-3 2-chloromethylpyridine hydrochloride 
• 790235-36-8 4-nitro-N-(2-pyridin-2-yl-ethyl)-N-pyridin-2-ylmethyl-benzenesulfonamide 
• 111195-90-5 4-nitro-N-(pyridin-2-ylmethyl)benzenesulfonamide 
• 3731-51-9 2-(Aminomethyl)pyridine 
• 1121-60-4 pyridine-2-carbaldehyde 
• 138938-20-2 2-(pyridin-2-yl)ethyl(pyridin-2-ylmethylene)amine 
• 100-69-6 2-vinylpyridine 
• 103-74-2 2-(2-Hydroxyethyl)pyridine 

Downstream Products

• 167415-73-8 4-Nitro-2-{[(2-pyridin-2-yl-ethyl)-pyridin-2-ylmethyl-amino]-methyl}-phenol 
• 790235-37-9 C₅₁H₄₉N₅O₁₁S 
• 1242440-92-1 4-bromo-2-(1,4-dimethyl-1,4,7-triazacyclononane-7-ylmethyl)-6-{[N-(2-pyridyl)methyl-N-2-(2-pyridylethyl)amine]-methyl}phenol 
• 1363651-63-1 C₂₁H₂₃N₅O₂ 
• 1363652-92-9 C₂₂H₂₅N₅O₃ 
• 1346110-27-7 C₄₀H₄₀N₈ 
• 1402045-93-5 N-(2-(pyridin-2-yl)ethyl)-N-((pyridin-2-yl)methyl)benzamide 
• 1392139-14-8 4,6-bis[N-(2-pyridylmethyl)-N-(2-(2-pyridyl)ethyl)aminomethyl]-2-phenylpyrimidine 
• 1442651-33-3 C₂₅H₃₁N₃O₂ 

Relevant articles and documents

Synthesis and characterization of FeIII(μ-OH)ZnII complexes: Effects of a second coordination sphere and increase in the chelate ring size on the hydrolysis of a phosphate diester and DNA

The synthesis and characterization of three ligands and their respective heterobinuclear FeIIIZnII complexes were carried out, with the goal of mimicking the active site of purple acid phosphatases (PAPs). The ligand 2-hydroxy-3-(((2-hydroxy-5-methyl-3-(((2-(pyridin-2-yl)ethyl)(pyridin-2-ylmethyl)amino)methyl)benzyl)(pyridin-2ylmethyl)amino)methyl)-5-methylbenzaldehyde (H2L2) was synthesized and its complex (FeIIIZnIIL2) was used as a basis for comparison with similar complexes previously published in the literature. Subsequent modifications were conducted in the aldehyde group, where 1,2-ethanediamine and 1,4-diaminobutane were used as side chain derivatives. The compounds FeIIIZnIIL2 (1), FeIIIZnIIL2-et (2) and FeIIIZnIIL2-but (3) were characterized by spectroscopic methods (infrared and UV-Vis) and ESI-MS spectrometry. Theoretical calculations were performed to provide insights into the complex structures with FeIIIZnII structures. The hydrolytic activity was analyzed both with the model substrate 2,4-BDNPP and with DNA catalyzed by complexes 1, 2 and 3.

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DNA binding, nuclease activity and cytotoxicity studies of Cu(ii) complexes of tridentate ligands

Cu(ii) complexes of three tridentate ligands, L1, L2 and L3, [L1, N-((1H-imidazole-2-yl)methyl)-2-(pyridine-2- yl)ethanamine; L2, N-((1-methyl-1H-imidazole-2-yl)methyl)-2- (pyridine-2-yl)ethanamine; L

Preparation of the Ru3(CO)8-pyridine-alcohol cluster and its use for the selective catalytic transformation of primary to secondary amines

The synthesis of pyridine alcohol based ruthenium carbonyl clusters Ru3(hep)2(CO)8 (1), Ru3(hpp)2(CO)8 (2), and Ru3(bhmp-H)2(CO)8 (3) {hep-H = 2-(2-hydroxyethyl)pyridine, hpp-H = 2-(3-hydroxypropyl)pyridine and bhmp-H2 = 2,6-bis(hydroxymethyl)pyridine} has been carried out by the reaction of the corresponding pyridine-alcohol ligands with Ru3(CO)12. Clusters 1-3 have been characterized using elemental analysis, NMR, FT-IR, mass spectrometry and single-crystal X-ray structures. The clusters were explored for the selective catalytic transformation of primary amines into secondary amines using alcohols as the mono-alkylating agents via hydrogen transfer reactions. All three display efficient catalytic activity with 1 being the most effective.