Interesting facts
Interesting Facts About 2-Chloro-4,6-Dinitro-Aniline
2-Chloro-4,6-dinitro-aniline, commonly known for its significant role in scientific research and industrial applications, is an intriguing compound in the field of chemistry. Here are some fascinating insights about this compound:
- Explosive Potential: This compound is often associated with its reactivity and potential use in explosives. The presence of nitro groups (-NO2) in its structure contributes to its energetic properties, which make it a subject of interest in the development of various energetic materials.
- Dye Manufacturing: 2-Chloro-4,6-dinitro-aniline is utilized in the synthesis of dyes. Its existing functional groups can be modified, allowing for the production of a wide array of colored compounds used in textiles and inks.
- Biological Implications: Some studies have indicated that this compound can exhibit biological activities. Its interaction with biological systems makes it a candidate for further research, especially in understanding how such compounds can serve as pharmaceuticals or pesticides.
- Structural Significance: The compound’s structure, featuring both chlorine and nitro groups attached to an aniline base, illustrates the concept of electronic effects in organic chemistry. The electronegative chlorine atom and the electron-withdrawing nitro groups significantly influence the reactivity and stability of the molecule.
- Environmental Considerations: As with many nitrogen-containing compounds, the environmental impact is a critical consideration. The potential for this compound to degrade in the environment and its toxicity to living organisms necessitate careful handling and disposal practices in industrial settings.
In summary, 2-chloro-4,6-dinitro-aniline is not just a compound of academic interest; it embodies the intersection of synthetic chemistry, environmental science, and industrial application. As chemists continue to explore its properties, one can only wonder what new discoveries await!
Synonyms
2-Chloro-4,6-dinitroaniline
3531-19-9
6-Chloro-2,4-dinitroaniline
Benzenamine, 2-chloro-4,6-dinitro-
CCRIS 3112
EINECS 222-564-9
QJ874UC2KK
2,4-dinitro-6-chloroaniline
BRN 2463157
ANILINE, 6-CHLORO-2,4-DINITRO-
ANILINE, 2-CHLORO-4,6-DINITRO-
DTXSID6063062
3-12-00-01718 (Beilstein Handbook Reference)
DINITRO-6-CHLOROANILINE, 2,4-
DTXCID2038994
222-564-9
(2-chloro-4,6-dinitrophenyl)amine
6-Chloro-2,4-dinitroanilene
MFCD00007147
UNII-QJ874UC2KK
6-chloro-2,4-dinitro-aniline
SCHEMBL1501666
6-Chloro-2,4-dinitroaniline, 97%
AKOS005111051
AC-11796
AS-75670
DB-048779
CS-0323386
NS00022085
D89282
SR-01000004768
SR-01000004768-1
F0020-1806
InChI=1/C6H4ClN3O4/c7-4-1-3(9(11)12)2-5(6(4)8)10(13)14/h1-2H,8H
Solubility of 2-chloro-4,6-dinitro-aniline
2-chloro-4,6-dinitro-aniline, commonly referred to as 2C4D, presents unique solubility characteristics that are essential to its application in various chemical processes. This compound is known for its limited solubility in water, which can pose challenges in certain formulations. Here’s a brief overview:
In summary, while 2-chloro-4,6-dinitro-aniline is predominantly insoluble in water, its behavior in organic solvents provides opportunities for various applications. Understanding these solubility properties is crucial for effectively utilizing this compound in laboratory and industrial settings.