CAS 4531-79-7
:3-Nitrodiphenylamine
Description:
3-Nitrodiphenylamine is an organic compound characterized by its structure, which consists of two phenyl rings connected by an amine group and a nitro group positioned on one of the phenyl rings. This compound typically appears as a solid and is known for its yellow to orange color. It is primarily used in the production of dyes, pigments, and as an intermediate in the synthesis of various organic compounds. The presence of the nitro group contributes to its reactivity, making it a potential candidate for further chemical transformations. 3-Nitrodiphenylamine is also noted for its applications in the field of rubber and polymer chemistry, where it can act as an antioxidant. However, like many nitro compounds, it may pose environmental and health risks, necessitating careful handling and disposal. Its physical properties, such as solubility and melting point, can vary based on purity and specific conditions. Overall, 3-Nitrodiphenylamine is a significant compound in both industrial and research settings.
Formula:C12H10N2O2
InChI:InChI=1/C12H10N2O2/c15-14(16)12-8-4-7-11(9-12)13-10-5-2-1-3-6-10/h1-9,13H
Synonyms:- 3-NITRO-N-PHENYLBENZENAMINE
- 3-nitro-N-phenylaniline
- Benzenamine,3-nitro-N-phenyl-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
3-Nitro-N-phenylaniline
CAS:3-Nitro-N-phenylaniline is a monosubstituted aniline derivative that is optimal for the synthesis of 3-nitrosobenzene. It has been shown to react with sodium carbonate in an acidic medium at room temperature to produce sodium nitrite and benzoic acid. The reaction time for this process depends on the substituent effects on the aromatic ring. The protonation of the nitro group leads to the formation of nitrous acid, which can be detected by its fluorescence. 3-Nitro-N-phenylaniline is synthesized from phenylhydrazine and formaldehyde in an inorganic setting with constant stirring.
Formula:C12H10N2O2Purity:Min. 95%Molecular weight:214.22 g/mol
