69824-99-3

Usage

Uses

Used in Dye and Pigment Production:
2,6-dinitrobenzene-1,4-dicarboxylic acid is used as a key intermediate in the synthesis of various dyes and pigments. Its unique chemical structure allows for the creation of a wide range of colors and properties, making it an essential component in the production of high-quality dyes and pigments.
Used in Organic Synthesis:
2,6-dinitrobenzene-1,4-dicarboxylic acid is used as a building block in organic synthesis for the construction of more complex chemical compounds. Its high reactivity enables the formation of various functional groups and molecular structures, making it a versatile starting material for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
2,6-dinitrobenzene-1,4-dicarboxylic acid is used as a research tool in the development of new materials and chemical processes. Its unique properties and reactivity make it an ideal candidate for studying reaction mechanisms, exploring new synthetic routes, and discovering novel applications in various fields.
Used in Medical Research:
2,6-dinitrobenzene-1,4-dicarboxylic acid has been studied for its potential as a treatment for certain medical conditions. Its chemical properties and reactivity may offer new therapeutic opportunities, and ongoing research aims to explore its potential applications in medicine.

Upstream product

• 610-29-7 2-nitroterephthalic acid 
• 609-92-7 2,5-dimethyl-1,3-dinitrobenzene 
• 859448-75-2 2-isopropyl-5-methyl-1,3-dinitro-benzene 
• 16533-71-4 3,5-dinitro-p-toluic acid 
• 99068-90-3 5-isopropyl-2-methyl-1,3-dinitro-benzene 
• 7697-37-2 nitric acid 
• 7664-93-9 sulfuric acid 
• 861571-04-2 3-(4-methyl-3,5-dinitro-phenyl)-glutaric acid 

Downstream Products

• 35111-99-0 2,6-dinitro-terephthalic acid-4-ethyl ester 
• 99069-07-5 2,6-diamino-terephthalic acid dimethyl ester 
• 1311280-46-2 dimethyl 2,6-bis(benzyloxycarbonylamino)terephthalate 

Relevant academic research and scientific papers

Method for synthesizing 2,6-dinitroterephthalic acid (by machine translation)

The reaction solution is subjected to post-treatment 2,6 - to obtain,dinitroterephthalic acid: and then the reaction solution is heated to, for, minutes, and then the reaction solution is heated to a reflux reaction 30 °C for, hours after the reaction sys

Synthesis of bis(propargyl) aromatic esters and ethers: A potential replacement for isocyanate based curators

This study reports the synthesis and characterization of a novel class of non-isocyanate curing agents based on bis-propargyl aromatic esters 2a-e and ethers 4a-c. A total of eight non-isocyanate curators were prepared from the reaction of respective dicarboxy or dihydroxybenzene with propargyl bromide in the presence of potassium carbonate with good yields. The structure and purity of the synthesized compounds and the corresponding intermediates were confirmed by spectral (IR and NMR), thermal (DSC) and chromatographic techniques (HPLC & GC-MS). Furthermore, kinetics of the curing reaction between glycidyl azide polymer (GAP) and the synthesized alkynes (4b, 4c) were studied using time-resolved FT-IR spectroscopy as a function of time at 303, 323 and 333 K. It was found that the curing reaction was faster when the temperature was increased. Kinetic parameters of the curing reaction, such as the reaction order and activation energy, were calculated for the GAP-4a and GAP-4c systems. All the curing reactions followed first order kinetics and the corresponding activation energy of the curing reaction for the systems was found to be 15.56 and 13.22 kcal mol-1. For comparison, curing studies were performed for GAP with a conventional curator Desmodur N-100. GAP cured with non-isocyanate curators offered good mechanical properties compared to GAP cured with isocyanate (N-100). The advantage of these new curing systems is that they do not require catalyst and there is no need for specific environmental conditions. Based on these studies, 1,4-bis(2-propynyloxy)benzene (4b) has the most potential as a non-isocyanate curator for azide polymeric binders.

A small fluorophore reporter of protein conformation and redox state

A new thiol-specific reagent introduces a small bis(methylamino) terephthalic acid fluorophore into proteins. The noninvasive probe with distinct spectroscopic properties offers many advantages for protein labeling, purification, and mechanistic work prom