25877-30-9

Usage

Uses

Used in Coordination Chemistry:
N,N-Diethyl-N-[2-(2-pyridyl)ethyl]amine is used as a ligand in coordination chemistry for forming complexes with metal ions. Its basic properties and ability to coordinate with metals make it a valuable component in the development of new materials with specific properties and applications.
Used in Organic Synthesis:
In the field of organic synthesis, N,N-diethyl-N-[2-(2-pyridyl)ethyl]amine serves as an intermediate for the synthesis of various organic compounds. Its reactivity in oxidation and substitution reactions allows for the creation of a wide range of chemical products, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Industry:
N,N-Diethyl-N-[2-(2-pyridyl)ethyl]amine may also find applications in the pharmaceutical industry, potentially serving as a building block for the development of new drugs or as a component in drug delivery systems. Its chemical properties and reactivity make it a candidate for further exploration in medicinal chemistry.
Used in Chemical Research:
As a chemical compound with unique properties, N,N-diethyl-N-[2-(2-pyridyl)ethyl]amine is utilized in chemical research to study its reactivity, stability, and potential applications in various chemical processes. Researchers may investigate its interactions with other compounds and its role in catalytic reactions or as a template for the synthesis of new materials.

InChI:InChI=1/C11H18N2/c1-3-13(4-2)10-8-11-7-5-6-9-12-11/h5-7,9H,3-4,8,10H2,1-2H3

Upstream product

• 100-69-6 2-vinylpyridine 
• 109-89-7 diethylamine 
• 103-74-2 2-(2-Hydroxyethyl)pyridine 
• 660-68-4 diethyl amine hydrochloride 
• 5351-04-2 3-diethylaminopropionitrile 
• 74-86-2 acetylene 
• 109-06-8 α-picoline 
• 7647-01-0 hydrogenchloride 
• 50-00-0 formaldehyd 
• 107-13-1 acrylonitrile 
• 22320-32-7 2-(2-pyridinyl)-ethyl 4-methylbenzenesulfonate 
• 7732-18-5 water 
• 16927-00-7 2-(2-chloroethyl)pyridine 

Downstream Products

• 100-69-6 2-vinylpyridine 

Relevant academic research and scientific papers

Synthesis, structures of (aminopyridine)nickel complexes and their use for catalytic ethylene polymerization

A series of α-aminopyridines in the form of (2,6-C6H 3N)(R1)(CHR2NR3R4) (R1 = R2 = H R3 = H R4 = iPr (L1a), R4 = tBu (L1b), R4 = Ph (L1c), R4 = 2,6-Me2C6H3 (L1d), R4 = 2,6-iPr2C6H3 (L1e), R1 = R2 = H R3 = R4 = Et (L1f), R1 = H R2 = Me R3 = H R4 = iPr (L2a), R4 = Ph (L2c), R4 = 2,6-Me 2C6H3 (L2d), R4 = 2,6- iPr2C6H3 (L2e), R1 = Me R2 = H R3 = H R4 = 2,6-iPr 2C6H3 (L3e)) and β-aminopyridines in the form of (2-C6H4N)(CH2CH2NR 1R2) (R1 = H R2 = iPr (4a), R2 = tBu (L4b), R1 = R2 = Et (L4f)) have been prepared. Their corresponding halonickel complexes 1a-4f are synthesized by ligand substitution from (DME)NiBr2 and the molecular structures are characterized. Four types of coordination modes include four-coordinate mononuclear species with one ligand, five-coordinate mononuclear species with two ligands, five-coordinate dinuclear species with two ligands, and a six-coordinate polymeric framework were determined by X-ray crystallography. Using methylaluminoxanes (MAO) as the activator, the nickel complexes can catalyze ethylene polymerization under moderate pressure and ambient temperature. The activity reaches 105 g PE mol-1 Ni h. The PE products with high branching and high crystallinity have M n ～ 103 with PDI 2.

Synthesis of some quaternary ammonium alkylating agents and their effects on soman-inhibited acetylcholinesterase

A number of compounds were synthesized and tested for their ability to realkylate the phosphonate anion of 'aged', soman-inhibited acetylcholinesterase. None were found able to do so, but two of the compounds in particular, [2-(4-pyridyl)ethyl]diethylmethylammonium iodide and its 2-isomer, proved able to slow the rate of aging significantly.

SYNTHESIS OF FUNCTIONALLY SUBSTITUTED PYRIDINES AND DIPYRIDYL-SUBSTITUTED COMPOUNDS WITH THE AID OF LOW-VALENCE COMPOLEXES

The possibility of the preparation of oxygen, nitrogen, and sulfur-containing pyridines and dipyridyl-substituted compounds by the cyclocotrimerization of substituted propionitriles with acetylene under the influence of a Co(2-ethylhexanoate)2-Al(C2H5)3 catalyst was demonstrated.It was established that the nature of the heteroatom in substituted propionitriles has virtually no effect on the direction of the reaction.

Process for the catalytic production of 2-substituted pyridines

A process for the catalytic production of a 2-substituted pyridine which comprises reacting a corresponding cyano compound and acetylene in the presence of cobaltocene. Favorable conversion speed, conversion of at least 90 percent, good yield and high selectivity are obtained.