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Phenacyl chloride

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Identification
Molecular formula
C8H9ClS
CAS number
5535-49-9
IUPAC name
2-chloroethylsulfanylbenzene
State
State

At room temperature, 2-Chloroethylsulfanylbenzene is typically found as a liquid. It should be handled carefully due to its volatile nature.

Melting point (Celsius)
-41.00
Melting point (Kelvin)
232.15
Boiling point (Celsius)
272.00
Boiling point (Kelvin)
545.15
General information
Molecular weight
156.68g/mol
Molar mass
156.6470g/mol
Density
1.0962g/cm3
Appearence

2-Chloroethylsulfanylbenzene is a colorless to pale yellow liquid. It has a distinct pungent odor and may appear slightly oily.

Comment on solubility

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:

  • Moderate solubility in organic solvents: It readily dissolves in non-polar solvents like hexane and diethyl ether due to its hydrophobic aromatic ring.
  • Poor solubility in water: The presence of both a chlorine atom and a sulfanyl group may lead to limited interactions with water molecules, thus resulting in low solubility.

Factors Influencing Solubility

Several factors can affect the solubility of 2-chloroethylsulfanylbenzene:

  • Temperature: Increased temperatures generally enhance solubility in organic solvents.
  • Polarity of the solvent: The type of solvent plays a crucial role; polar solvents will not dissolve this compound effectively, whereas non-polar solvents will do so more readily.
  • Concentration of the compound: At higher concentrations, the solubility may also vary due to intermolecular interactions.

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.

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