39753-68-9

Usage

Imidazoline derivative

A chemical compound based on the imidazoline ring structure.

Synthesis of pharmaceuticals

Used as an intermediate in the production of various pharmaceutical compounds.

Organic compound synthesis

Utilized in the creation of other organic compounds.

Chelating agent potential

Capable of binding to metal ions, which can be useful in various chemical processes.

Corrosion inhibitor potential

Suggests the ability to prevent or reduce corrosion in materials.

Applications in chemistry

Due to its unique structure and properties, it can be used in various chemical reactions and processes.

Applications in materials science

The potential use in preventing corrosion and its chelating properties can benefit the development of new materials.

Unique structure

The combination of imidazoline ring and various substituents (hydroxy, phenyl, and methyl groups) contributes to its distinct properties.

Upstream product

• 39753-69-0 2,2,5,5-tetramethyl-4-phenyl-3-imidazolin-1-oxyl 
• 57327-98-7 4-dichloromethyl-2,2,5,5-tetramethyl-3-imidazoline-3-oxide-1-oxyl 
• 917-64-6 methyl magnesium iodide 
• 259672-14-5 2-methoxy-4,4-dimethyl-5-phenyl-4H-imidazole 3-oxide 
• 183194-84-5 2,2-dimethyl-5-methoxy-4-phenyl-2H-imidazol 1-oxide 
• 18796-03-7 4-phenyl-2,2,5,5-tetramethyl-3-imidazolin-1-yloxy-3-oxide 
• 122-66-7 diphenyl hydrazine 
• 302-15-8 methylhydrazine hemisulfate 

Downstream Products

• 104110-44-3 1-acetoxy-2,2,5,5-tetramethyl-4-phenyl-3-imidazoline 
• 39753-69-0 2,2,5,5-tetramethyl-4-phenyl-3-imidazolin-1-oxyl 
• 160983-47-1 C₂₀H₂₁N₂O₂ 

Relevant academic research and scientific papers

Reactions of cyclic α-methoxy nitrones with nucleophilic reagents

Reactions of cyclic α-methoxy nitrones, which are derivatives of imidazole or dihydroimidazole N-oxides, with amines, KOH, or KSH result in the replacement of the MeO group to form cyclic α-amino nitrones, hydroxamic acids, or thiohydroxamic acids, respectively. Analogous reactions occur with C-nucleophiles.

EFFECT OF THE CHEMICAL STRUCTURE OF NITROXYL RADICALS ON THEIR REACTIVITY IN THE REACTION WITH HYDRAZOBENZENE AND TETRANITROMETHANE

The reaction rate constants of reduction of stable radicals of different classes by hydrazobenzene in hexane at ca. 20 deg C, in the range of 0.4 - 5*103 M-1 sec-1, were determined; a single scale of the oxidative properties of stable nitroxyl radicals was constructed.The rate constants of oxidation of a series of nitroxyl radicals by tetranitromethane in aqueous medium at ca. 20 deg C, in the range of 0.06 - 10 M-1 sec-1, were determined.It was shown that the oxidative properties of the nitroxyl group decrease slightly with an increase in its reducing properties for nitroxyl radicals of the piperidine and imidazoline series in reactions with ascorbic acid and tetranitromethane in aqueous medium, respectively.

The Oxidative Properties of Nitroxy-radicals in Their Reactions with Sterically Hindered Hydroxylamines

A relative scale of the oxidative properties of cyclic nitroxy-radicals has been constructed and the influence of various structural factors on the oxidising capacity of the nitroxy-group in the radicals has been investigated.It is shown that the oxidative properties of the nitroxy-group in cyclic nitroxy-radicals become more pronounced with the increase in ring size.A relation has been established between the oxidative properties and the electron-accepting properties of functional groups separated from the nitroxy-group by two and more ?-bonds.