6633-30-3

Usage

Uses

Used in Dye and Pigment Production:
4-Iodo-2,6-dinitrotoluene is used as a chemical intermediate in the production of dyes and pigments. Its unique chemical structure allows for the creation of a wide range of colors and shades, making it a valuable component in this industry.
Used in Explosive Manufacturing:
4-Iodo-2,6-dinitrotoluene is also used in the manufacturing of explosives due to its high energy content and reactivity. Its properties make it suitable for use in various explosive formulations, contributing to its effectiveness in these applications.
Used in Chemical Research:
In addition to its industrial uses, 4-iodo-2,6-dinitrotoluene is also utilized in chemical research for the development of new compounds and materials. Its unique properties and reactivity make it a valuable tool for scientists and researchers in the field of chemistry.

InChI:InChI=1/C7H5IN2O4/c1-4-6(9(11)12)2-5(8)3-7(4)10(13)14/h2-3H,1H3

Upstream product

• 19406-51-0 4-Amino-2,6-dinitrotoluene 
• 606-20-2 2,6-dinitrotoluene 
• 118-96-7 2,4,6-Trinitrotoluene 

Downstream Products

• 6942-35-4 5-iodo-2-methyl-3-nitroaniline 
• 798567-87-0 5-iodo-2-methylbenzene-1,3-diamine 
• 1058142-23-6 phenyl [1-(1-benzyl-1H-indazol-6-yl)pyrrolidin-2-one]-4-ylcarbamate 
• 1058142-21-4 1-(1-benzyl-4-nitro-1H-indazol-6-yl)pyrrolidin-2-one 
• 1058142-22-5 1-(4-amino-1-benzyl-1H-indazol-6-yl)pyrrolidin-2-one 
• 1058142-20-3 1-benzyl-6-iodo-4-nitro-1H-indazole 
• 29302-69-0 3.5-Dijodo-2-methylanilin 
• 10388-22-4 4,6-diiodo-2-nitrotoluene 
• 36994-79-3 2,4,6-triiodo-toluene 
• 798567-82-5 2,6-bis[3,4,5-tri(3,7-(S)-dimethyl-octyloxy)-benzoylamino]-4-trimethylsilylethynyl-toluene 
• 798567-80-3 2,6-bis[3,4,5-tri(3,7-(S)-dimethyl-octyloxy)-benzoylamino]-4-iodo-toluene 
• 95192-58-8 4-iodo-2,6-dinitrobenzoic acid 

Relevant academic research and scientific papers

Molecular Engineering onto RuIIBis(1,2-diphenylphosphinoethane) Synthon: Toward an Original Organometallic Gelator

In this article, we report the successful molecular engineering of Ru bis-acetylides that led for the first time to a gelator and more specifically in aromatic solvents. By means of a nonlinear ligand and an extended aromatic platform, the bulky Ru bis-ac

Deciphering the potentiometric properties of (porphinato)zinc(ii)-derived supramolecular polymers and related superstructures

Because modulating the structure-function relationships of π-conjugated superstructures opens fresh opportunities to tune the electronic structures of semiconducting materials, self-assembled architectures have emerged as pivotal candidates to engineer optoelectronic devices. While the photophysical and electrical properties of 1-dimensional supramolecular polymers have been extensively explored, establishing their fundamental potentiometric properties using reliable electrochemical measurements has been less scrutinized and would benefit the engineering of semiconducting materials. In this regard, elucidating the energy level of valence and conduction bands that delineate the electronic structure of self-assemblies is critical to unveiling the parameters that regulate their structure-function properties. In the present contribution, design principles to engineer 2-dimensional nanosheets, nanowires, fibers and amorphous solids from (porphinato)zinc(ii) (PZn) building blocks have been elucidated by modifying the structural properties of the side chains that flank PZn-based cores. As these self-assemblies feature identical redox-active building blocks but evidence different solid-state morphologies, the elucidation of their potentiometric properties reveals important structural parameters that regulate the potentials at which holes and electrons are injected into the valence and conduction bands of these hierarchical materials. While self-assembly conformations modestly impact valence band energies, superstructures built from H-type aggregates feature a conduction band energy stabilized by more than 350 meV with respect to those constructed from J-type aggregates.

Superelectrophilic iodination of deactivated arenes with triiodoisocyanuric acid

The reaction of triiodoisocyanuric acid (TICA) with deactivated arenes in acidic medium led to the efficient and regioselective formation of the corresponding iodoarenes, in 55-88% isolated yield. The acidity of the medium was found to be the most important factor influencing the electrophilic iodination of weakly nucleophilic substrates by TICA. Georg Thieme Verlag Stuttgart New York.

INDAZOLE DERIVATIVES AND THEIR USE AS VANILLOID RECEPTOR LIGANDS

The present invention relates to indazole derivatives of the following formula I, which can be used as vanilloid receptor ligands, processes for their preparation, and their use in treating diseases, conditions and/or disorders modulated by vanilloid receptors. (I)