Interesting facts
Interesting Facts about 2,6-dichloroaniline
2,6-dichloroaniline is an aromatic amine that has garnered interest in various fields of chemistry, particularly in organic synthesis and materials science. This compound derives its name from its structure, where two chlorine atoms are substituted at the 2 and 6 positions of the aniline ring. Here are some captivating insights about this chemical:
- Versatile Intermediate: 2,6-dichloroaniline is widely used as an important intermediate in the synthesis of azo dyes, which are characterized by their bright colors and application in textiles. Such dyes contribute significantly to the modern fashion industry.
- Pharmaceutical Relevance: The compound serves as a precursor for various pharmaceuticals, showcasing its role in drug development. Its derivatives exhibit potential biological activities, making it a subject of research in medicinal chemistry.
- Environmental Impact: As with many chlorinated compounds, 2,6-dichloroaniline poses environmental and health concerns. Understanding its pathways and the potential for bioaccumulation is crucial for mitigating its risks in ecological contexts.
- Research Applications: Scientists often utilize it in studies focused on substitution reactions and the reactivity of aromatic compounds. Its unique electronic characteristics due to the chlorine substituents make it an ideal candidate for exploring reaction mechanisms.
- Safety Measures: Given its potential toxicological effects, proper handling and storage are essential when working with 2,6-dichloroaniline. Awareness of safety protocols ensures the wellbeing of both researchers and the environment.
In conclusion, 2,6-dichloroaniline serves as an example of how a simple chemical structure can lead to multifaceted applications and considerations in chemistry. As research progresses, the compound continues to hold promise within both industrial and academic realms.
Synonyms
2,6-DICHLOROANILINE
Benzenamine, 2,6-dichloro-
2,6-dichlorobenzenamine
2,6-Dichloranilin
2,6-dichlorophenylamine
KG3RW7NW6M
CHEBI:46630
ANILINE, 2,6-DICHLORO-
DICHLOROANILINE, 2,6-
DTXSID5044449
CLONIDINE HYDROCHLORIDE IMPURITY C [EP IMPURITY]
CLONIDINE HYDROCHLORIDE IMPURITY C (EP IMPURITY)
DTXCID3024449
210-160-5
inchi=1/c6h5cl2n/c7-4-2-1-3-5(8)6(4)9/h1-3h,9h
jdmfxjulngepoi-uhfffaoysa-n
608-31-1
MFCD00007675
2,6-Dichloro-Phenylamine
2,6-dichloro aniline
EINECS 210-160-5
Clonidine Hydrochloride Imp. C (EP); Clonidine Imp. C (EP); 2,6-Dichloroaniline; Clonidine Hydrochloride Impurity C; Clonidine Impurity C
2,6-dichloro-aniline
UNII-KG3RW7NW6M
(2,6-dichlorophenyl)amine
2,6-bis(chloranyl)aniline
SCHEMBL71630
CHEMBL28368
(2,6-dichloro-phenyl)-amine
2,6-Dichloroaniline, >=98%
STR01943
STL264184
AKOS000119117
PS-3007
AC-10710
DB-024161
D0323
NS00009798
EN300-19071
F52576
2,6-Dichloroaniline 100 microg/mL in Methanol
A832913
Q2145677
2,6-Dichloroaniline, PESTANAL(R), analytical standard
F0001-1593
Solubility of 2,6-Dichloroaniline
2,6-Dichloroaniline, with the chemical formula C6H5Cl2N, exhibits unique solubility characteristics in various solvents.
Solvent Behavior
In terms of solubility:
Factors Influencing Solubility
Several factors affect the solubility of 2,6-dichloroaniline:
In conclusion, the solubility of 2,6-dichloroaniline is notably higher in organic solvents compared to water, demonstrating essential implications for its applications in various chemical processes.