Interesting facts
Interesting Facts about (4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene
(4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene, often simply referred to in the chemical community as a notable member of the diazene derivatives, carries a unique structure that highlights the versatility of azobenzenes. Here are several intriguing points about this compound:
- Structural Complexity: This compound features an azobenzene core, incorporating a diazene group (–N=N–) which plays a crucial role in its reactivity and properties. The presence of multiple chlorine substituents increases the electron-withdrawing character, enhancing the compound's stability under certain conditions.
- Applications in Material Science: Due to its unique electronic properties, this compound is often studied for applications in photonic materials and photoresponsive systems. The alterations in electronic structure upon light exposure can enable innovative technologies, such as light-driven switches.
- Biological Significance: Compounds with similar structures have garnered attention in medicinal chemistry. They often exhibit interesting biological activities, which can include anti-cancer properties or potential use as imaging agents in biological systems.
- Environmental Considerations: As chlorinated compounds can be persistent in the environment, the study of this compound also extends to its degradation pathways and their implications for ecotoxicology. Understanding how such compounds behave can inform safety and remediation strategies.
- Research Frontiers: The rich chemistry surrounding diazenes has made them a focal point in organic synthesis and materials research. The exploration of their reactivity under different conditions continues to provide vital insights into new synthetic methodologies.
This compound exemplifies the intersection of chemistry and applied science, demonstrating how synthetic compounds can lead to significant advancements in both academic research and practical applications. Its complexities remind us of the intricate dance between structure and function in chemical compounds.
Synonyms
Chlorfensulfide
2274-74-0
Chlorfensulphide
Azosulfide
Chlorfensulphide [ISO]
(4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene
66B1G5582O
CPAS
Chlorfensulfid [German]
Chlorfensulfid
BRN 1843651
UNII-66B1G5582O
4-Chlorophenyl 2,4,5-trichlorophenylazosulfide
2,4,5-Trichlorophenylazo-4'-chlorophenyl-sulfide
p-Chlorfenyl-2,4,5-trichlorfenylazosulfid [Czech]
Benzenediazo p-chlorophenyl sulfide, 2,4,5-trichloro-
4-Chlorphenyl-2',4',5'-trichlorphenylazosulfid [German]
p-Chlorfenyl-2,4,5-trichlorfenylazosulfid
DIIMIDE, ((p-CHLOROPHENYL)THIO)(2,4,5-TRICHLOROPHENYL)-
4-Chlorphenyl-2',4',5'-trichlorphenylazosulfid
SCHEMBL163403
DTXSID0041771
CHEBI:82156
DTXSID00859712
NS00122554
C19025
Q27155773
4-CHLOROPHENYL 2,4,5-TRICHLOROPHENYLAZO SULFIDE
Diazene, ((4-chlorophenyl)thio)(2,4,5-trichlorophenyl)-
(E)-[(4-CHLOROPHENYL)SULFANYL](2,4,5-TRICHLOROPHENYL)DIAZENE
Solubility of (4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene
The solubility of (4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene can be influenced by several factors, including its chemical structure and the nature of its functional groups. Here are some key points to consider:
In summary, the solubility of (4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene is likely to be moderate in non-polar solvents but limited in water due to the combined effects of its chlorinated groups and overall hydrophobic character. This reaffirms the classic principle of "like dissolves like" in chemistry.