CAS 6393-42-6
:4-Methyl-2,6-dinitroaniline
Description:
4-Methyl-2,6-dinitroaniline, with the CAS number 6393-42-6, is an organic compound belonging to the class of anilines, which are characterized by the presence of an amino group (-NH2) attached to an aromatic ring. This particular compound features two nitro groups (-NO2) and a methyl group (-CH3) on the benzene ring, contributing to its chemical reactivity and properties. It typically appears as a yellow crystalline solid and is known for its relatively low solubility in water, while being more soluble in organic solvents. The presence of multiple nitro groups enhances its potential as a precursor in the synthesis of various dyes and explosives. Additionally, 4-Methyl-2,6-dinitroaniline exhibits moderate toxicity, necessitating careful handling and appropriate safety measures during use. Its chemical structure allows for various reactions, including nitration and reduction, making it a versatile compound in organic synthesis. As with many nitroanilines, it may pose environmental hazards, emphasizing the importance of proper disposal and management practices.
Formula:C7H7N3O4
InChI:InChI=1/C7H7N3O4/c1-4-2-5(9(11)12)7(8)6(3-4)10(13)14/h2-3H,8H2,1H3
InChI key:InChIKey=MOOOPNRPJGZXPE-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(N)C(N(=O)=O)=CC(C)=C1
Synonyms:- (4-Methyl-2,6-dinitrophenyl)amine
- 1-Amino-2,6-dinitro-4-methylbenzene
- 2,6-Dinitro-P-Toluidine
- 4-Amino-3,5-dinitrotoluene
- 4-Methyl-2,6-Dinitroaniline
- 4-Methyl-2,6-dinitrobenzenamine
- Benzenamine, 4-methyl-2,6-dinitro-
- NSC 97354
- p-Toluidine, 2,6-dinitro-
- 2,6-Dinitro-4-methylaniline
- 4-Fluoro-2,6-dinitroaniline
- 2,6-Dinitro-p-toluidine (NH2=1)
- Benzenamine, 4-methyl-2,6-dinitro- (9CI)
- 4-methyl-2,6-dinitro-aniline
- Amino-2,6-dinitrotoluene, 4-: (4-Amino-3,5-dinitrotoluene)
- See more synonyms
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Found 2 products.
(4-Methyl-2,6-dinitrophenyl)amine
CAS:Formula:C7H7N3O4Purity:95%Color and Shape:SolidMolecular weight:197.14822,6-Dinitro-4-methylaniline
CAS:<p>2,6-Dinitro-4-methylaniline is an amide that has been shown to induce cancer in animals. It has a high affinity for nucleic acids and forms covalent bonds with DNA. 2,6-Dinitro-4-methylaniline is metabolized by the liver and excreted by the kidneys into urine, where it can be detected in urine samples. This compound has been shown to bioconcentrate in organisms and accumulate in tissues as well as activate radiation. The activation of this compound is dose dependent and may be due to its ability to form covalent bonds with DNA.</p>Formula:C7H7N3O4Purity:Min. 95%Color and Shape:PowderMolecular weight:197.15 g/mol

