Interesting facts
Interesting Facts About 4-(4-amino-2,5-dichloro-phenyl)-2,5-dichloro-aniline
4-(4-amino-2,5-dichloro-phenyl)-2,5-dichloro-aniline is a fascinating organic compound that belongs to the class of anilines, which are characterized by the presence of an amino group (-NH2) attached to an aromatic ring. Here are some interesting aspects of this compound:
- Biological Significance: Anilines are often found in various biological systems. This specific compound has potential applications in pharmaceuticals, particularly due to its potential antitumor properties.
- Synthesis: The synthesis of this compound involves multiple steps of electrophilic substitution reactions, showcasing the importance of reactivity in aromatic compounds. This provides a valuable learning opportunity about reaction mechanisms in organic chemistry.
- Environmental Concerns: The presence of chlorine atoms in its structure raises environmental and health concerns, as chlorinated compounds can be persistent in the environment and may have detrimental effects on ecosystems.
- Chemical Reactivity: The amino group (-NH2) often serves as a site for further reactions, making this compound a versatile intermediate in organic synthesis. It can contribute to the production of dyes, agrochemicals, and more.
- Research Usage: Compounds similar to this one are often used as intermediates to develop more complex molecules, making it a staple in laboratories exploring advanced materials or pharmaceuticals.
This compound exemplifies the synergy between structure and function in organic chemistry, making it a compound of interest not only for chemists but also for those in the fields of environmental science and medicine. Its complex structure and potential applications underscore the importance of understanding such compounds in the broader context of scientific research.
Synonyms
2,2',5,5'-TETRACHLOROBENZIDINE
15721-02-5
3,3',6,6'-Tetrachlorobenzidine
Benzidine, 2,2',5,5'-tetrachloro-
[1,1'-Biphenyl]-4,4'-diamine, 2,2',5,5'-tetrachloro-
ICS5PD3141
DTXSID7021314
(1,1'-Biphenyl)-4,4'-diamine, 2,2',5,5'-tetrachloro-
DTXCID601314
2,2'5,5'-TCB
239-815-3
Tetrachlorobenzidine
2,2,5,5-Tetrachlorobenzidine
2,2',5,5'-Tetrachloro-[1,1'-biphenyl]-4,4'-diamine
4-(4-amino-2,5-dichlorophenyl)-2,5-dichloroaniline
MFCD00043918
2,2',5,5'-Tetrachloro-4,4'-diaminodiphenyl
4,4'-Diamino-2,2',5,5'-tetrachlorobiphenyl
CHEBI:82540
2,2',5,5'-Tetrachloro-(1,1'-biphenyl)-4,4'-diamine
C12H8Cl4N2
CAS-15721-02-5
EINECS 239-815-3
4-(4-amino-2,5-dichlorophenyl)-2,5-dichlorophenylamine
BRN 3364286
UNII-ICS5PD3141
2,2',5,5'-tetrachlorobiphenyl-4,4'-diamine
YSWG728
3-13-00-00447 (Beilstein Handbook Reference)
SCHEMBL142135
2,2',5,5'-Tetrachloro(1,1'-biphenyl)-4,4'-diamine
CHEMBL3186078
UXOXUHMFQZEAFR-UHFFFAOYSA-
MSK1288
QAA72102
Tox21_202027
Tox21_302911
SBB071659
2,2\',5,5\'-Tetrachlorobenzidine
AKOS009031249
CS-W009887
NCGC00249152-01
NCGC00256382-01
NCGC00259576-01
AC-33840
AS-69025
SY052209
DB-043346
NS00025110
ST45026751
T0933
TETRACHLOROBENZIDINE, 2,2',5,5'-
EN300-21420
C19533
H10725
2,2',5,5'-TETRACHLOROBENZIDINE [IARC]
Q27156051
4-(4-amino-2,5-dichloro-phenyl)-2,5-dichloro-aniline
2,2',5,5'-Tetrachloro[1,1'-biphenyl]-4,4'-diamine #
2,2 inverted exclamation mark ,5,5 inverted exclamation mark -Tetrachlorobenzidine
InChI=1/C12H8Cl4N2/c13-7-3-11(17)9(15)1-5(7)6-2-10(16)12(18)4-8(6)14/h1-4H,17-18H2
Solubility of 4-(4-amino-2,5-dichloro-phenyl)-2,5-dichloro-aniline
The solubility of 4-(4-amino-2,5-dichloro-phenyl)-2,5-dichloro-aniline in various solvents presents notable characteristics. Understanding its solubility is essential for both practical applications and theoretical insights.
As a general rule: “Like dissolves like”. In this case, the increased hydrophobicity of the dichlorophenyl groups greatly limits the solubility in aqueous conditions. This highlights the importance of understanding the molecular structure when predicting solubility behaviors.
Overall, the solubility profile of this compound is crucial for its application in various fields, including pharmaceuticals, where solubility can affect bioavailability and efficacy.