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Usage

Uses

Used in Textile Industry:
2,6-Diethyl-3-nitroaniline is used as a dye in the textile industry for coloring various materials, taking advantage of its solubility in organic solvents and its ability to impart a distinct color to fabrics.
Used in Plastics Industry:
In the plastics industry, 2,6-Diethyl-3-nitroaniline serves as a coloring agent, enhancing the visual appeal of plastic products by providing them with a specific hue.
Used in Histology and Cytology:
2,6-Diethyl-3-nitroaniline is used as a staining reagent in histology and cytology for the detection and visualization of lipids, waxes, and triglycerides within cells and tissues, aiding in the study of cellular structures and functions.
Used in Lipid Detection:
2,6-Diethyl-3-nitroaniline is utilized for the detection of both saturated and unsaturated lipids in cells and tissues, playing a crucial role in biological and medical research, as well as in diagnostic applications.
Used in Pharmaceutical Research:
Although not yet a mainstream application, 2,6-Diethyl-3-nitroaniline has been studied for potential use in pharmaceuticals due to its interaction with lipid molecules, which could lead to the development of new drugs or drug delivery systems targeting lipid-related conditions.

Upstream product

• 579-66-8 2,6-diethylaniline 
• 16665-89-7 N-(2,6-diethylphenyl)acetamide 
• 91557-77-6 acetic acid-(2,6-diethyl-3-nitro-anilide) 

Relevant academic research and scientific papers

Enantiospecific Synthesis of Nepetalactones by One-Step Oxidative NHC Catalysis

An efficient oxidative NHC-catalyzed one-step transformation of (S)-or (R)-8-oxocitronellal to nepetalactone (NL) in enantio- A nd diastereomerically pure form has been developed. Several new and "easy to make" N-Mes-or N-Dipp-substituted 1,2,4-triazolium salts carrying nitroaromatic groups on N1 were synthesized and evaluated as precatalysts in combination with base and stoichiometric organic oxidant. Under optimized conditions, NLs are accessible in very good yields and diastereomerically pure under mild conditions. The oxidant used could be recovered and recycled under operationally simple conditions.

C5A RECEPTOR ANTAGONISTS

The present invention is related to a compound, preferably a C5a receptor antagonist, having the following structure, Rl, R2, R3, R4, R5, R6, R7, R8, R9, Rl0, RI l, R12, R13, R14, R15, R16, Rl7, R18, Rl9, R20, R21 and R22 are individually and independently selected from the group comprising H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, heterocyclyl, substituted heterocyclyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl, heteroarylalkyl, substituted heteroarylalkyl, alkoxyl, substituted alkoxyl, aryloxy, substituted aryloxy, arylalkyloxy, substituted arylalkyloxy, acyloxy, substituted acyloxy, halogen, hydroxyl, nitro, cyano, acyl, substituted acyl, mercapto, alkylthio, substituted alkylthio, amino, substituted amino, alkylamino, substituted alkylamino, bisalkyl amino, substituted bisalkyl amino, cyclic amino, substituted cyclic amino, carbamoyl (-CONH2), substituted carbamoyl, carboxyl, carbamate, alkoxycarbonyl, substituted alkoxycarbonyl, acylamino, substituted acylamino, sulfamoyl (-SO2NH2), substituted sulfamoyl, haloalkyl, haloalkyloxy, -C(O)H, trialkylsilyl and azido.

Synthesis of Indoles via Ring Closure of 2-Alkylnitroaniline Derivatives.

A variety of nitroindoles have been prepared from imidate, amidine, and sec-anilide derivatives of 2-alkyl-3- or 5-nitroanilines by a base-induced cyclization promoted by dialkyl oxalates.It is shown that essentially the same procedure also can be used to synthesize the corresponding nitroindole-3-glyoxylates in one simple operation.The synthetic potential is discussed and a mechanism is proposed.

Revisitation of Formaldehyde Aniline Condensation. VIII. - Monomeric N-Methylene Anilines

A convenient, high yield "dry" method of synthesis of monomeric N-methyleneanilines (6a-i) and the characterization of the products by m.s., 1H- and 13C-n.m.r. and i.r. are reported, improving previous procedures and describing new compounds.It appeared that the existence of monomeric N-methyleneanilines is stricly related to the presence of enough steric hindrance to oligomerization by substituents in ortho positions.Moreover, some addition products of formaldehyde to an amine and its corresponding imines are tentatively identified on the basis of the observed mass spectrum of the whole reaction mixture.The reaction products of formaldehyde with 2,6-dimethylaniline (1a) provided an example of a mobile equilibrium between monomeric and trimeric imine.