19779-32-9

Usage

Uses

Used in Epoxy and Polyurethane Resin Industry:
2,4,6-triethylaniline is used as a curing agent and accelerator for epoxy and polyurethane resins. It enhances the curing process and improves the mechanical and thermal properties of the final product.
Used in Coatings and Adhesives Industry:
2,4,6-triethylaniline is used as a hardening agent for certain types of coatings and adhesives. It provides increased durability and resistance to environmental factors.
Used in Agrochemical Industry:
2,4,6-triethylaniline is used in the production of herbicides and fungicides. It contributes to the effectiveness of these products in controlling unwanted plant growth and preventing fungal infections.
Used in Dye and Pharmaceutical Synthesis:
2,4,6-triethylaniline is used as an intermediate in the synthesis of dyes and pharmaceuticals. Its unique chemical structure allows for the creation of various compounds with specific properties.
However, it is important to note that 2,4,6-triethylaniline is classified as a hazardous substance. It should be handled with caution due to its potential health risks, including skin and eye irritation, respiratory effects, and potential carcinogenicity. Proper safety measures and personal protective equipment should be used during its handling and processing.

Upstream product

• 13402-30-7 2-nitro-1,3,5-triethylbenzene 
• 71-43-2 benzene 
• 64-19-7 acetic acid 
• 102-25-0 1,3,5-triethylbenzene 

Downstream Products

• 90936-32-6 benzoic acid-(2,4,6-triethyl-anilide) 
• 71757-46-5 1-Propyl-3-(2,4,6-triethyl-cyclohexyl)-thiourea 
• 68065-66-7 N-(2,4,6-Triaethylphenyl)-N'-isobutylthioharnstoff 
• 26953-05-9 N,N,N',N'-Tetramethyl-N'-<2,4,6-triethylphenyl>-guanidin 
• 116342-22-4 (R)-2-Phenyl-N-(2,4,6-triethyl-phenyl)-propionamide 
• 139418-63-6 azotriethylbenzene 
• 10330-39-9 2-Chloro-1,3,5-triethyl-4-fluoro-benzene 
• 10330-40-2 2-Bromo-1,3,5-triethyl-4-fluoro-benzene 
• 10330-41-3 1,3,5-Triethyl-2-fluoro-4-iodo-benzene 
• 1262942-39-1 (S)-N-(2,4,6-triethylbenzene)pyrrolidine-2-carboxamide 
• 1262942-43-7 (2S,4R)-4-hydroxy-N-(2,4,6-triethylphenyl)pyrrolidine-2-carboxamide 
• 69769-03-5 1-(3,3-Dimethyl-butyl)-3-(2,4,6-triethyl-phenyl)-thiourea 
• 68065-67-8 N-(2,4,6-Triaethylphenyl)-N'-neopentylthioharnstoff 

Relevant academic research and scientific papers

A Metal-Free Direct Arene C?H Amination

The synthesis of aryl amines via the formation of a C?N bond is an essential tool for the preparation of functional materials, active pharmaceutical ingredients and bioactive products. Usually, this chemical connection is only possible by transition metal-catalyzed reactions, photochemistry or electrochemistry. Here, we report a metal-free arene C?H amination using hydroxylamine derivatives under benign conditions. A charge transfer interaction between the aminating reagents TsONHR and the arene substrates enables the chemoselective amination of the arene, even in the presence of various functional groups. Oxygen was crucial for an effective conversion and its accelerating role for the electron transfer step was proven experimentally. In addition, this was rationalized by a theoretical study which indicated the involvement of a dioxygen-bridged complex with a “Sandwich-like” arrangement of the aromatic starting materials and the aminating agents at the dioxygen molecule. (Figure presented.).

Enantioselective organocatalytic Biginelli reaction: Dependence of the catalyst on sterics, hydrogen bonding, and reinforced chirality

From a systematic investigation involving the synthesis of a series of catalysts and screening studies, the organocatalyst 16, which is sterically hindered, contains a strong hydrogen-bonding site, and is endowed with reinforced chirality, is shown to pro

Migrations in Oxidations of Mesidine

The oxidation of mesidine in methanolic media by ferricyanide, dichromate, and persulfate afforded an anil 4 containing a shifted methoxymethyl group in addition to the principal anil 3 formed by oxidative dealkylation.Possible intermediates 6, 7, and 8 were prepared and oxidized to the product anils.Oxidations of related anilines 9, 10, and 13 did not parallel those of mesidine but afforded analogues of 3.There is significant spectral evidence for anils with alkyl shifts but little for anils analogous to 4.