34322-82-2

Usage

Uses

Used in Pharmaceutical Industry:
N-(2-Methoxyethyl)ethylamine is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, enhancing their efficacy and properties.
Used in Agrochemical Industry:
In the agrochemical sector, N-(2-Methoxyethyl)ethylamine is utilized as an intermediate in the production of agrochemicals. Its role in the synthesis process contributes to the development of effective and targeted agricultural products.
Used as a Solvent:
N-(2-Methoxyethyl)ethylamine is employed as a solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it a valuable component in the manufacturing of different products.
Used in Surfactant and Dispersant Production:
This chemical compound is also used in the production of surfactants and dispersants. Its properties enable it to improve the performance of these products, enhancing their ability to stabilize and disperse substances in various applications.

InChI:InChI=1/C5H13NO/c1-3-6-4-5-7-2/h6H,3-5H2,1-2H3

Upstream product

• 42988-04-5 N-ethyl-N-(2-methoxyethyl)aniline 
• 75-04-7 ethylamine 
• 6482-24-2 2-Bromoethyl methyl ether 
• 5417-42-5 N-(2-methoxyethyl)acetamide 
• 75-07-0 acetaldehyde 
• 109-85-3 2-methoxyethylamine 

Downstream Products

• 7404-72-0 N-ethyl-N-(2-methoxyethyl)acetamide 
• 1027590-10-8 N-ethyl-N-(2-methoxy-ethyl)-2-methyl-5-nitro-N'-(2,4,6-trimethyl-phenyl)-pyrimidine-4,6-diamine 
• 209333-68-6 8-(4-Benzyloxy-phenyl)-7-oxo-7H-thieno[2,3-a]quinolizine-10-carboxylic acid ethyl-(2-methoxy-ethyl)-amide 
• 209334-05-4 7-Oxo-8-(4-phenoxy-phenyl)-7H-thieno[2,3-a]quinolizine-10-carboxylic acid ethyl-(2-methoxy-ethyl)-amide 
• 1224595-18-9 C₂₃H₂₉FN₂O₅ 

Relevant academic research and scientific papers

Benzothiazole derivatives with activity as adenosine receptor ligands

The present invention relates to substituted benzothiazole derivitives and to their pharmaceutically acceptable salts useful for the treatment of diseases related to the adenosine receptor.

ELECTROCHEMICAL REDUCTIVE AMINATION. II. AMINATION OF ALIPHATIC ALDEHYDES WITH PRIMARY AMINES

The formation of a secondary amine by the electrolysis of an aqueous solution containing an aldehyde and a primary amine was studied.The formation of the secondary amines passes through the intermediate stage of an aldimine.The highest yield of secondary amine is attained at a molar ratio of primary amine to aldehyde of 1.2:1.As electrode material lead, cadmium, zinc, and copper may be used.As supporting electrolyte a phosphate buffer with a pH close to the pKa of the primary amine is recommended.By the method developed 32 amines with various structures were synthesized.

CONFIGURATIONAL BIASING OF TERTIARY AMIDE IONOPHORES BY ALKALI METAL CHELATION1,2.

Configurational analysis can be used as a probe for association constants for chelation of amides with alkali metals. Carbon-13 NMR spectroscopy indicates that tertiary amides, each bearing a triethylene oxide substituent at nitrogen, exist as a mixture of E and Z isomers. Addition of alkali metal cation (KSCN) increases the concentration of species with the Z configuration since this configuration can chelate potassium ion. High-field **1H NMR spectra have been used to determine the chelation constants for amides in the presence of KSCN. It has been determined that (a) the carbonyl oxygen is involved in chelation and (b) the number of ether oxygens on the substituent at nitrogen is the significant factor in the chelating ability of these ionophores.