74209-44-2

Usage

Uses

Used in Chemical Industry:
2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as a reagent in organic synthesis for its ability to form stable complexes with metal ions, which aids in various chemical reactions and processes.
Used in Pharmaceutical Research:
In pharmaceutical research, 2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as a building block for the development of new pharmaceuticals, leveraging its complex-forming properties to enhance drug design and effectiveness.
Used in Coordination Chemistry:
2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as a ligand in coordination chemistry to create stable metal complexes, which have potential applications in various fields such as catalysis, materials science, and medicinal chemistry.
Used in Metal Ion Extraction Processes:
In metal ion extraction processes, 2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as an extracting agent to selectively bind and separate metal ions from solutions, which is crucial in environmental remediation and industrial applications.
Used in Production of Pharmaceuticals:
2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as an intermediate in the production of various pharmaceuticals, contributing to the synthesis of active ingredients and improving drug efficacy.
Used in Agrochemicals:
In the agrochemical industry, 2,2-Diethoxy-2-(4-pyridyl)ethylamine is used in the development of new agrochemicals, such as pesticides and herbicides, where its complex-forming ability can enhance the performance and selectivity of these products.

InChI:InChI=1/C11H18N2O2/c1-3-14-11(9-12,15-4-2)10-5-7-13-8-6-10/h5-8H,3-4,9,12H2,1-2H3

Upstream product

• 64-17-5 ethanol 
• 107445-22-7 (E)-1-(pyridin-4-yl)ethanone O-tosyloxime 
• 917-58-8 potassium ethoxide 
• 74209-52-2 4-(1-tosyloxyimino)ethylpyridine 
• 1122-54-9 methyl (4-pyridyl) ketone 
• 107445-21-6 (E)-1-(pyridin-4-yl)ethan-1-one oxime 

Downstream Products

• 151427-23-5 N-<2,2-diethoxy-2-(4-pyridyl)ethyl>-4-methoxybenzamide 
• 151426-99-2 2-(4-methoxyphenyl)-5-(4-pyridyl)oxazole 
• 151427-24-6 N-<2-keto-2-(4-pyridyl)ethyl>-4-methoxybenzamide 
• 521087-64-9 1-(4-fluorophenyl)-5-(pyridin-4-yl)-4-imidazolin-2-one 
• 701298-22-8 4-(2-Ethyl-1H-imidazol-4-yl)pyridine 
• 521091-68-9 C₂₂H₁₆FN₃O₂ 
• 521087-65-0 1-cyclopentylmethyl-3-(4-fluorophenyl)-4-(pyridin-4-yl)-4-imidazolin-2-one hydrochloride 
• 220444-97-3 7-chloro-9-(4-nitro-phenyl)-1-pyridin-4-yl-4H-3,10,10a-triaza-benzo[f]azulene 
• 304647-10-7 7-bromo-9-(4-nitro-phenyl)-1-pyridin-4-yl-4H-3,10,10a-triaza-benzo[f]azulene 

Relevant academic research and scientific papers

Efficient synthesis of 2-imidazol-2-ylacetates

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.

4-IMIDAZOLIN-2-ONE COMPOUNDS

The present invention relates to a compound of the formula [I] : ???wherein G1 is an alkyl which,may be substituted by a halogen atom or an alkoxy, or a group of the formula: ??????wherein ring B is benzene ring which may be substituted, etc.,