Interesting facts
Interesting Facts About 3-Nitro-N-(4-nitrophenyl)aniline
3-Nitro-N-(4-nitrophenyl)aniline, often referred to in scientific literature as a substituted aniline derivative, is a fascinating compound with a variety of applications and implications in different fields. Here are some intriguing insights:
- Chemical Structure: This compound features two nitro groups attached to a phenyl ring, which significantly influences its chemical reactivity and properties.
- Applications: It finds utility in organic synthesis, primarily in the development of dyes and pigments due to its vibrantly colored properties.
- Biological Activity: Research has shown that derivatives of aniline compounds sometimes exhibit antibacterial and antifungal properties, making them candidates for pharmaceutical advancements.
- Environmental Impact: Due to the presence of nitro groups, compounds like 3-nitro-N-(4-nitrophenyl)aniline can pose risks to the environment and human health, necessitating careful handling and disposal methods.
- Analytical Use: Its structure can be utilized in analytical chemistry as a standard in chromatographic techniques, helping scientists in the quantification of similar compounds in various matrices.
In conclusion, the study of 3-nitro-N-(4-nitrophenyl)aniline not only sheds light on its unique chemical properties but also underscores the broader importance of understanding nitro-substituted anilines in both industrial and environmental contexts. As a scientist or a student of chemistry, exploring such compounds reveals the intricate balance between utility and safety in the field of chemical research.
Synonyms
3-NITRO-N-(4-NITROPHENYL)BENZENAMINE
15979-87-0
DTXSID30166729
DTXCID0089220
3-nitro-N-(4-nitrophenyl)aniline
AKOS000286161
Solubility of 3-nitro-N-(4-nitrophenyl)aniline
The solubility of 3-nitro-N-(4-nitrophenyl)aniline, a compound featuring both nitro groups and an aniline structure, is influenced by its chemical characteristics. Being an organic nitrogen compound, it exhibits variable solubility in different solvents, primarily due to the presence of polar nitro groups which can engage in hydrogen bonding.
Factors Affecting Solubility
However, despite these attributes, the overall solubility may be limited due to:
As a general observation, compounds like 3-nitro-N-(4-nitrophenyl)aniline tend to have increased solubility in organic solvents (e.g., ethanol, acetone) compared to water, but actual solubility can vary significantly depending on temperature and specific solvent conditions.
Understanding the solubility of this compound is crucial for applications in organic synthesis and pharmaceuticals, where the ability to dissolve effectively can dictate reaction pathways and efficacy.