Benzenamine, 2,3-dimethyl-6-nitro-


Chemical Name: Benzenamine, 2,3-dimethyl-6-nitro-
CAS Number: 59146-96-2
Product Number: AG003FK5(AGN-PC-0JTIUR)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties


Properties
MP:
117-120 °C(lit.)
BP:
334.3°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.6273 (estimate)
Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
71.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
178
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


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Chemical Structure



2,3-Dimethyl-6-nitroaniline is a versatile compound commonly used in chemical synthesis. It serves as a valuable building block for the production of a wide range of organic compounds due to its unique reactivity and structural properties.One key application of 2,3-Dimethyl-6-nitroaniline is in the synthesis of various dyes and pigments. Its nitro group can undergo various chemical transformations, allowing for the introduction of different functional groups and modifications to tailor the properties of the final dye or pigment. This compound is particularly useful in the preparation of azo dyes, which are known for their vibrant colors and wide applications in textiles, printing, and other industries.Additionally, 2,3-Dimethyl-6-nitroaniline is utilized in the synthesis of pharmaceutical intermediates. Its molecular structure provides a platform for the creation of complex molecules with specific biological activities. By incorporating this compound into the synthesis of pharmaceuticals, chemists can access new potential drug candidates and optimize the efficacy and safety profiles of existing medications.Moreover, 2,3-Dimethyl-6-nitroaniline can be employed in the preparation of organic synthesis catalysts. Its nitroaniline framework can serve as a ligand for coordinating with transition metals, enabling the development of efficient catalyst systems for various chemical reactions. These catalysts play a crucial role in accelerating reactions, improving selectivity, and enhancing the overall efficiency of organic synthesis processes.In summary, 2,3-Dimethyl-6-nitroaniline is a valuable compound in chemical synthesis, serving as a key building block for the production of dyes, pigments, pharmaceutical intermediates, and catalysts. Its versatility and reactivity make it a crucial component in the toolbox of synthetic chemists seeking to develop novel compounds with tailored properties and applications.