6633-30-3

Basic information

• Product Name: 4-IODO-2,6-DINITROTOLUENE
• Synonyms: Benzene, 5-iodo-2-methyl-1,3-dinitro-
• CAS NO: 6633-30-3
• Molecular Formula: C₇H₅IN₂O₄
• Molecular Weight: 308.0301
• Mol File: 6633-30-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 342°Cat760mmHg
• Flash Point: 160.6°C
• Appearance: /
• Density: 2.033g/cm³
• Vapor Pressure: 0.000153mmHg at 25°C
• Refractive Index: 1.677
• CAS DataBase Reference: 4-IODO-2,6-DINITROTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-IODO-2,6-DINITROTOLUENE(6633-30-3)
• EPA Substance Registry System: 4-IODO-2,6-DINITROTOLUENE(6633-30-3)

Safety Data

• Hazardous Substances Data: 6633-30-3(Hazardous Substances Data)

Usage

General Description

4-Iodo-2,6-dinitrotoluene is a compound with the chemical formula C7H5N3O4I, and it is a derivative of toluene. It is commonly used in the production of dyes and pigments, as well as in the manufacturing of explosives. 4-IODO-2,6-DINITROTOLUENE is considered to be toxic and may cause skin and eye irritation upon contact. Additionally, it is highly flammable and should be handled and stored with caution. Overall, 4-iodo-2,6-dinitrotoluene is a chemical used in various industrial processes, but it poses potential health and safety risks if not managed properly.

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

Upstream product

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

Downstream Products

• 6942-35-4 5-iodo-2-methyl-3-nitroaniline 
• 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 
• 798567-87-0 5-iodo-2-methylbenzene-1,3-diamine 
• 95192-58-8 4-iodo-2,6-dinitrobenzoic acid 
• 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 

Relevant articles and documents

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

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.