Interesting facts
Interesting Facts about 2-Chloroethylsulfanylbenzene
2-Chloroethylsulfanylbenzene, often referred to as a simple aromatic thioether, presents a range of intriguing properties and applications that chemists and researchers find noteworthy. Here are some fascinating aspects of this compound:
- Structural Significance: The presence of both a chloro group and a sulfanyl group in this aromatic compound allows for unique reactivity patterns, making it an important building block in synthetic organic chemistry.
- Versatile Reactivity: This compound can undergo various chemical reactions, such as nucleophilic substitutions and electrophilic aromatic substitutions, which are fundamental in the creation of more complex molecules.
- Applications in Pharmaceuticals: Compounds similar to 2-chloroethylsulfanylbenzene have been investigated for their potential use in pharmaceuticals due to their ability to modify biological activities, thereby influencing drug design.
- Involvement in Polymer Science: Its unique thiol functional group enables it to participate in polymerization reactions, making it relevant in the development of new materials.
- Environmental Implications: As a chlorinated compound, 2-chloroethylsulfanylbenzene may pose environmental concerns, highlighting the importance of understanding its degradation pathways and potential toxicity.
In summary, the study of 2-chloroethylsulfanylbenzene not only expands our knowledge of aromatic compound behavior but also drives innovation across multiple fields, from pharmaceuticals to material science. As noted by chemists, “The simplicity of structure often belies the complexity of reactivity.” This compound is a perfect example of how a simple modification can lead to a wealth of possibilities in chemical synthesis and application.
Synonyms
[(2-chloroethyl)thio]benzene
Benzene, [(2-chloroethyl)thio]-
((2-CHLOROETHYL)THIO)BENZENE
Benzene, ((2-chloroethyl)thio)-
EINECS 226-891-8
NSC 45458
DTXSID10203904
DTXCID00126395
Benzene, ((2-chloroethyl)thio)-(9CI)
226-891-8
2-Chloroethyl phenyl sulfide
5535-49-9
(2-chloroethyl)(phenyl)sulfane
2-chloroethylsulfanylbenzene
[(2-Chloroethyl)sulfanyl]benzene
2-(Phenylthio)ethyl chloride
MFCD00013691
2-Chloroethylphenylsulfide
NSC45458
2-phenylthioethylchloride
(2-chloroethylthio)benzene
1-chloro-2phenylthioethane
1-chloro-2-phenylthioethane
SCHEMBL123612
(2-chloro-ethyl) phenyl sulfide
CS-M0048
[(2-Chloroethyl)sulfanyl]benzene #
2-Chloroethyl phenyl sulfide, 98%
NSC-45458
AKOS005206771
SY049286
DB-052719
NS00033300
EN300-51949
A830603
Q26840736
Solubility of 2-Chloroethylsulfanylbenzene
2-Chloroethylsulfanylbenzene, also known as 2-(Chloroethylthio)toluene, exhibits unique solubility characteristics that are essential to understand for its applications in various chemical processes.
General Solubility Behavior
This compound demonstrates:
Factors Influencing Solubility
Several factors can affect the solubility of 2-chloroethylsulfanylbenzene:
In summary, 2-chloroethylsulfanylbenzene's solubility is determined by its molecular structure and the solvent used. As with many organic compounds, understanding these solubility traits is vital for optimizing reactions and formulations in practical applications.