Interesting facts
Exploring 2,6-Dinitro-4-(trifluoromethyl)aniline
2,6-Dinitro-4-(trifluoromethyl)aniline is an intriguing compound known for its multifaceted applications and unique chemical properties. Here are some interesting facts about this chemical:
- Chemical Structure: This compound features a nitro group and a trifluoromethyl group, which contribute to its distinctive reactivity and physical properties. The presence of multiple electron-withdrawing groups can significantly influence the compound's behavior in various reactions.
- Applications: It is often utilized in the synthesis of more complex organic molecules and operates as a versatile intermediate in the chemical industry. Its derivatives may be used in pharmaceuticals and agrochemicals, underscoring its importance in both fields.
- Environmental and Safety Considerations: While working with this compound, safety is paramount. Many nitroaniline derivatives, including this one, may pose risks due to their potential toxicity and environmental impact. Proper handling and disposal are essential to ensure lab safety and environmental protection.
- Yellow Color: Compounds similar to 2,6-dinitro-4-(trifluoromethyl)aniline typically exhibit vibrant colors, making them useful in dyestuff applications. This visual characteristic can aid in quickly identifying the presence of such compounds in various mixtures.
- Synthesis: The synthesis of this compound can be executed through various methods, including nitration and halogenation reactions. Chemistry students often appreciate the mechanistic pathways that lead to such complex structures, providing insight into the broader principles of organic synthesis.
In summary, 2,6-dinitro-4-(trifluoromethyl)aniline is a compound that not only serves practical purposes in industry but also presents a fascinating study subject for students and professionals alike. Its unique structure and reactivity illustrate fundamental chemical principles while highlighting the significance of diligence in handling chemicals safely.
Synonyms
2,6-Dinitro-4-(trifluoromethyl)aniline
445-66-9
4-Amino-3,5-dinitrobenzotrifluoride
UNII-P9BDZ5UC73
2,6-Dinitro-4-(trifluoromethyl)benzenamine
P9BDZ5UC73
2,6-dinitro-4-trifluoromethylaniline
Benzenamine, 2,6-dinitro-4-(trifluoromethyl)-
DTXSID70196202
.alpha.,.alpha.,.alpha.-Trifluoro-2,6-dinitro-p-toluidine
a,a,a-Trifluoro-2,6-dinitro-p-toluidine
p-Toluidine, .alpha.,.alpha.,.alpha.-trifluoro-2,6-dinitro-
p-Toluidine, a,a,a-trifluoro-2,6-dinitro-
SCHEMBL9015339
DTXCID40118693
AAA44566
MFCD00024260
STK839148
AKOS001023666
4-Amino-3,5-dinitrobenzotrifluoride, 97%
DB-051231
CS-0313525
1C-124
G77478
SR-01000196757
alpha,alpha,alpha-Trifluoro-2,6-dinitro-p-toluidine
SR-01000196757-1
p-Toluidine, alpha,alpha,alpha-trifluoro-2,6-dinitro-
Q27286411
Z56757038
626-240-1
Solubility of 2,6-Dinitro-4-(trifluoromethyl)aniline
2,6-Dinitro-4-(trifluoromethyl)aniline, known for its distinctive structure, presents intriguing solubility characteristics. Understanding its solubility involves examining various factors that impact how well it can dissolve in different solvents:
Consequently, one might say, "Like dissolves like," indicating that compounds with similar polarities are more likely to dissolve in each other. In summary, 2,6-dinitro-4-(trifluoromethyl)aniline exhibits interesting solubility properties influenced by its molecular structure and the nature of the solvent used. Understanding these factors is essential for applications in pharmaceuticals and materials science.