Interesting facts
Phenyl(p-tolyl)diazene: An Intriguing Compound
Phenyl(p-tolyl)diazene is a fascinating compound that has captivated the attention of chemists due to its unique structure and properties. This compound is essentially an azobenzene derivative, featuring a diazene functional group that introduces distinct characteristics and potential applications.
Key Characteristics
- Mesomeric Effects: The presence of two aromatic rings contributes to a significant amount of resonance stabilization. This makes the compound relatively stable compared to other diazenes.
- Photochromism: Like many azobenzene derivatives, phenyl(p-tolyl)diazene can undergo isomerization upon exposure to light. This property makes it useful in photoresponsive materials and molecular switches.
- Biological Activities: Research has shown that some diazene derivatives exhibit anti-cancer properties. Their ability to interact with biological molecules opens new avenues for drug design.
Applications in Science and Technology
Phenyl(p-tolyl)diazene serves as a versatile building block in organic synthesis. Here are a few notable applications:
- Used as a dye in textile industries due to its vibrant color changes.
- Involved in the development of photonic devices, which utilize light to transmit information.
- Serves as a precursor to various chemical compounds used in pharmaceuticals.
In summary, phenyl(p-tolyl)diazene is not only a compound of academic interest but also a potential key player in various industrial applications. As scientists and students continue to explore its properties, this compound exemplifies the beauty and complexity of organic chemistry.
Synonyms
4-Methylazobenzene
EINECS 213-444-7
DTXSID90870815
1-(4-Methylphenyl)-2-phenyldiazene
NSC 31005
DTXCID80818504
213-444-7
p-Methylazobenzene
949-87-1
Azobenzene, 4-methyl-
Diazene, (4-methylphenyl)phenyl-
6720-39-4
Diazene, (4-methylphenyl)phenyl-, (E)-
Azobenzene, 4-methyl-, (E)-
NSC31005
(E)-1-(4-Methylphenyl)-2-phenyldiazene
CBDivE_003176
1-Phenyl-2-(p-tolyl)diazene
SCHEMBL1405529
GIJSVMOPNUOZBC-CCEZHUSRSA-N
GIJSVMOPNUOZBC-UHFFFAOYSA-N
(E)-1-Phenyl-2-(p-tolyl)diazene
NSC-31005
(E)-1-(4-Methylphenyl)-2-phenyldiazene #
NS00042460
10.14272/GIJSVMOPNUOZBC-CCEZHUSRSA-N.1
doi:10.14272/GIJSVMOPNUOZBC-CCEZHUSRSA-N.1
Solubility of Phenyl(p-tolyl)diazene
Phenyl(p-tolyl)diazene, with the chemical formula C13H12N2, presents unique solubility characteristics that are important for its application and utilization in various chemical processes. Here are some key points regarding its solubility:
In conclusion, the solubility of phenyl(p-tolyl)diazene is primarily influenced by its structure, which favors dissolution in non-polar organic environments while exhibiting substantial limitations in polar solvents such as water. Understanding these solubility properties is crucial for its effective application in organic synthesis and other chemical fields.