CAS 3460-29-5
:2,5-Dimethyl-4-nitrobenzenamine
Description:
2,5-Dimethyl-4-nitrobenzenamine, with the CAS number 3460-29-5, is an organic compound characterized by its aromatic amine structure. It features a benzene ring substituted with two methyl groups at the 2 and 5 positions and a nitro group at the 4 position, which significantly influences its chemical properties. This compound typically appears as a solid at room temperature and is known for its potential applications in dye synthesis and as an intermediate in organic synthesis. The presence of the nitro group contributes to its reactivity, making it a candidate for electrophilic substitution reactions. Additionally, the amine functional group can participate in various chemical reactions, including acylation and alkylation. 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 minimize exposure. Overall, 2,5-Dimethyl-4-nitrobenzenamine is a versatile compound with significant relevance in chemical research and industrial applications.
Formula:C8H10N2O2
InChI:InChI=1S/C8H10N2O2/c1-5-4-8(10(11)12)6(2)3-7(5)9/h3-4H,9H2,1-2H3
InChI key:InChIKey=PJAGNJQUIUEGKP-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(C)C=C(N)C(C)=C1
Synonyms:- 1-Amino-2,5-dimethyl-4-nitrobenzene
- 2,5-Dimethyl-4-nitroaniline
- 2,5-Dimethyl-4-nitrobenzenamine
- 2,5-Xylidine, 4-nitro-
- Aniline, 2,5-dimethyl-4-nitro-
- Benzenamine, 2,5-dimethyl-4-nitro-
- Benzenamine, 2,5-dimethyl-4-nitro- (9CI)
- Brn 2719183
- NSC 135156
- Nsc 43207
- 4-12-00-02573 (Beilstein Handbook Reference)
- See more synonyms
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Found 4 products.
2,5-Dimethyl-4-nitroaniline
CAS:Formula:C8H10N2O2Purity:95%Color and Shape:SolidMolecular weight:166.17722,5-Dimethyl-4-nitroaniline
CAS:<p>2,5-Dimethyl-4-nitroaniline</p>Color and Shape:SolidMolecular weight:166.18g/mol2,5-Dimethyl-4-nitroaniline
CAS:<p>2,5-Dimethyl-4-nitroaniline is an isomer of 2,5-dimethylaniline. The molecular electrostatic potential map reveals that the molecule has a high electron density at the 4 position of the aniline ring, which is characteristic of an aromatic system. This molecule displays a conformational change when it interacts with chloride ions, which can be seen in its vibrational spectrum. The nature of this molecule is interannular between aromatic and nonaromatic.<br>2,5-Dimethyl-4-nitroaniline's crystal system is orthorhombic. Its interactions with other molecules are determined by the electrostatic forces present on the surface of the crystal.</p>Formula:C8H10N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:166.18 g/mol



