52317-98-3

Usage

Uses

Used in Pharmaceutical Industry:
(1-ethylpropyl)methylamine(SALTDATA: HCl) is utilized as a building block or intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be incorporated into the development of drugs that target specific biological pathways or receptors, contributing to the creation of novel therapeutic agents.
Used in Chemical Manufacturing:
In the chemical manufacturing sector, (1-ethylpropyl)methylamine(SALTDATA: HCl) serves as a versatile intermediate for the production of specialty chemicals. Its reactivity and functional groups make it suitable for use in the synthesis of a range of chemical products, including surfactants, solvents, and other organic compounds that are integral to various industrial applications.

Upstream product

• 96-22-0 pentan-3-one 
• 74-89-5 methylamine 

Downstream Products

• 52317-72-3 3-(2,4-Dimethyl-phenyl)-1-(1-ethyl-propyl)-1-methyl-thiourea 
• 52403-60-8 3-(4-Chloro-2-methyl-phenyl)-1-(1-ethyl-propyl)-1-methyl-thiourea 

Relevant academic research and scientific papers

ELECTROCHEMICAL REDUCTIVE AMINATION. I. AMINATION OF ALIPHATIC KETONES BY PRIMARY AMINES

The reductive amination of aliphatic ketones in aqueous solutions of primary amines was realized by an electrochemical method.The best yields of the secondary amines were obtained at lead and cadmium cathodes in an aqueous electrolytic solution at pH 11-12.Elongation and branching in the carbon chain of the radicals both of the ketone and of the primary amine lead to a reduction in the yield of the secondary amine.The yield of the secondary amine is mainly determined by the rate of the chemical reaction leading to the formation of the azomethine compound, preceding the electrochemical reduction stage.

1,4-Dithiino[2,3-c; 6,5-c']diisothiazole and related compounds

The compound 3,7-dicyano-1,4-dithiino[2,3-c; 6,5-c']diisothiazole is prepared by reacting either tetracyano-1,4-dithiin or 4,5-dicyano-1,3-dithiolen-2-one with sulfur in 1,2-dimethoxyethane at a temperature of 50°-280° C in the presence of a basic catalyst. The diisothiazole can be converted to derivatives with various utilities, e.g., as fluorescent brighteners.