CAS 16947-63-0
:2,6-Dimethyl-4-nitrobenzenamine
Description:
2,6-Dimethyl-4-nitrobenzenamine, with the CAS number 16947-63-0, is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with two methyl groups and a nitro group, as well as an amino group. This compound typically appears as a solid at room temperature and is known for its yellow to orange color. It is a member of the aniline family, which are compounds containing an amino group attached to an aromatic ring. The presence of the nitro group introduces significant polarity and can influence the compound's reactivity, making it useful in various chemical syntheses and applications, including dyes and pigments. Additionally, the methyl groups contribute to its hydrophobic characteristics, affecting its solubility in different solvents. Safety considerations are important when handling this compound, as it may pose health risks, including potential toxicity and environmental hazards. Proper safety protocols should be followed to mitigate any risks associated with its use.
Formula:C8H10N2O2
InChI:InChI=1S/C8H10N2O2/c1-5-3-7(10(11)12)4-6(2)8(5)9/h3-4H,9H2,1-2H3
InChI key:InChIKey=NSBSVUUVECHDDX-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=CC(C)=C(N)C(C)=C1
Synonyms:- 2,6-Dimethyl-4-Nitroaniline
- 2,6-Dimethyl-4-nitro-phenylamine
- 2,6-Dimethyl-4-nitrobenzenamine
- 2,6-Dimethyl-4-nitrophenylamine
- 2,6-Xylidine, 4-nitro-
- 4-Nitro-2,6-Xylidine
- Benzenamine, 2,6-dimethyl-4-nitro-
- NSC 101580
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Found 5 products.
2,6-Dimethyl-4-nitroaniline
CAS:Formula:C8H10N2O2Purity:97%Color and Shape:SolidMolecular weight:166.17722,6-Dimethyl-4-nitroaniline
CAS:2,6-Dimethyl-4-nitroanilineFormula:C8H10N2O2Purity:95%Color and Shape: bright yellow solidMolecular weight:166.18g/mol2,6-Dimethyl-4-nitroaniline
CAS:Formula:C8H10N2O2Purity:97%Color and Shape:SolidMolecular weight:166.182,6-Dimethyl-4-nitroaniline
CAS:Controlled ProductFormula:C8H10N2O2Color and Shape:NeatMolecular weight:166.172,6-Dimethyl-4-nitroaniline
CAS:<p>2,6-Dimethyl-4-nitroaniline (DMN) is a nitrosamine that has been found to be a significant contaminant of drinking water. DMN is regulated as an irritant and a probable human carcinogen. The effects of DMN on the body are not fully understood, but it has been shown to cause damage to the liver and kidney in vivo. DMN may act by interfering with the synthesis of DNA or RNA, which can lead to cell death. The proposed mechanism for this is inhibition of the enzyme ribonucleotide reductase, which converts ribonucleotides into deoxyribonucleotides for DNA synthesis. This mechanism is supported by experiments in rats where DMN was found to inhibit erythrocyte production in vivo.<br>DMN can also be methylated in vivo by S-adenosylmethionine synthetase, yielding 2-methyl-6-dimethylamino-4</p>Formula:C8H10N2O2Purity:Min. 95%Molecular weight:166.18 g/mol




