Interesting facts
Interesting Facts about 2,6-Dichlorobenzene-1,4-Diamine
2,6-Dichlorobenzene-1,4-diamine, often referred to in scientific contexts for its unique structure and functional properties, is a compound with significant applications and intriguing characteristics. Here are some notable points to consider:
- Structure: This compound features two chlorine atoms and two amino groups positioned at specific locations on a benzene ring, contributing to its unique reactivity and properties.
- Versatile Intermediate: 2,6-Dichlorobenzene-1,4-diamine is commonly used as an intermediate in the synthesis of various dyes, pigments, and specialized polymers, making it valuable in industries such as textiles and paints.
- Biological Relevance: Some studies have indicated its potential interactions with biological systems, as certain derivatives might exhibit antibacterial or antifungal properties.
- Research Applications: This compound is often explored in research settings for developing new materials, particularly those that are heat-resistant or have specific electronic properties due to its nitrogen functional groups.
- Environmental Considerations: As with many chlorinated compounds, the environmental impacts of 2,6-dichlorobenzene-1,4-diamine must be carefully managed, especially concerning its stability and biodegradability in various ecosystems.
In summary, 2,6-dichlorobenzene-1,4-diamine is not just a compound with a complex nomenclature; it stands out due to its multifaceted roles in chemical synthesis, potential biological activities, and environmental implications. Its study can provide insights into both synthetic strategies and environmental sustainability.
Synonyms
2,6-Dichloro-1,4-phenylenediamine
609-20-1
2,6-Dichlorobenzene-1,4-diamine
2,6-Dichloro-p-phenylenediamine
Daito Brown Salt RR
2,6-DICHLORO-1,4-BENZENEDIAMINE
1,4-Diamino-2,6-dichlorobenzene
1,4-Benzenediamine, 2,6-dichloro-
NCI-C50260
2,5-Diamino-1,3-dichlorobenzene
2,6-Dichloro-para-phenylenediamine
p-Phenylenediamine, 2,6-dichloro-
3,5-Dichloro-1,4-phenylenediamine
CCRIS 226
NSC 60685
C.I. 37020
HSDB 4129
CI 37020
EINECS 210-184-6
Z4QJ0R1U1Z
BRN 2209257
DTXSID7020427
NSC-60685
DTXCID90427
4-13-00-00225 (Beilstein Handbook Reference)
4-AMINO-2,6-DICHLOROANILINE
2,6-DICHLORO-1,4-BENZENEDIAMINE [HSDB]
2,6-DICHLORO-PARA-PHENYLENEDIAMINE [IARC]
2,6-DICHLORO-PARA-PHENYLENEDIAMINE (IARC)
1,4Diamino2,6dichlorobenzene
2,5Diamino1,3dichlorobenzene
2,6Dichloro1,4benzenediamine
pPhenylenediamine, 2,6dichloro
2,6Dichloro1,4phenylenediamine
3,5Dichloro1,4phenylenediamine
1,4Benzenediamine, 2,6dichloro
210-184-6
inchi=1/c6h6cl2n2/c7-4-1-3(9)2-5(8)6(4)10/h1-2h,9-10h
Fast Brown RR Salt
CHEBI:82447
CAS-609-20-1
UNII-Z4QJ0R1U1Z
1,4-Benzenediamine,2,6-dichloro-
MFCD00025369
1,6-dichlorobenzene
2,4-phenylenediamine
3,4-phenylenediamine
WLN: ZR DZ BG FG
SCHEMBL292270
p-Phenylenediamine,6-dichloro-
CHEMBL551154
ALBB-024672
NSC60685
Tox21_201908
Tox21_302916
AKOS000120210
FD00633
PS-5124
NCGC00091148-01
NCGC00091148-02
NCGC00091148-03
NCGC00256501-01
NCGC00259457-01
DB-053740
CS-0102625
NS00001959
EN300-20648
C19399
Q27155947
Z104479464
2,6-Dichlorobenzene-1,4-diamine;3,5-Dichloro-1,4-phenylenediamine
Solubility of 2,6-Dichlorobenzene-1,4-diamine
2,6-Dichlorobenzene-1,4-diamine, a compound with the chemical formula C6H6Cl2N2, presents intriguing characteristics when it comes to solubility. Understanding its solubility behavior is crucial for various applications, particularly in the fields of organic chemistry and materials science. Here are some key points to consider:
Overall, the solubility of 2,6-dichlorobenzene-1,4-diamine is influenced by multiple factors, including the nature of the solvent, temperature, and pH of the solution. As such, it is vital to consider these variables when conducting experiments or applications involving this compound.