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Phenyl ethyl sulfide

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Identification
Molecular formula
C8H10S
CAS number
622-61-1
IUPAC name
ethylsulfanylbenzene
State
State

Phenyl ethyl sulfide is a liquid at room temperature.

Melting point (Celsius)
-32.00
Melting point (Kelvin)
241.15
Boiling point (Celsius)
243.00
Boiling point (Kelvin)
516.15
General information
Molecular weight
138.23g/mol
Molar mass
138.2330g/mol
Density
1.0235g/cm3
Appearence

Phenyl ethyl sulfide is a colorless to pale yellow liquid. It has a characteristic sweet and slightly sulfide odor.

Comment on solubility

Solubility of Ethylsulfanylbenzene

Ethylsulfanylbenzene, also known as thiophenol ethyl ether, exhibits a unique solubility profile that is influenced by its molecular structure. This compound is predominantly organic, leading to intriguing solubility characteristics:

  • Polar vs. Nonpolar Solvents: Ethylsulfanylbenzene is more soluble in nonpolar solvents compared to polar solvents. This is due to the presence of the ethylsulfanyl group, which enhances its hydrophobic nature.
  • Solvent Compatibility: It shows good solubility in organic solvents such as ethyl acetate, hexane, and benzene, while its solubility in water is quite limited.
  • Concentration Impact: As with many organic compounds, the solubility can vary with concentration and temperature; increasing temperature can lead to an increase in overall solubility in appropriate organic solvents.

In summary, the solubility of ethylsulfanylbenzene is key to its applicability in various chemical processes. Its preference for nonpolar environments highlights the importance of selecting the right solvent to optimize its use in reactions or extractions.

Interesting facts

Interesting Facts about Ethylsulfanylbenzene

Ethylsulfanylbenzene, commonly referred to as phenethyl sulfide, is an intriguing compound in the realm of organic chemistry. This aromatic compound is notable for its unique properties and applications. Here are some fascinating aspects:

  • Functional Group Importance: Ethylsulfanylbenzene contains a sulfanyl (thioether) group that plays a significant role in the reactivity and properties of the compound, allowing for interesting chemical transformations.
  • Natural Occurrence: Compounds similar to ethylsulfanylbenzene can be found in certain natural sources, contributing to the aroma and flavor profiles of various foods and plants.
  • Application in Synthesis: It is a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, where it serves as a building block for more complex structures.
  • Odor Characterization: The compound is noted for its distinct odor, which can sometimes resemble that of garlic or onions, making it an interesting study in olfactory chemistry.
  • Reactivity: Ethylsulfanylbenzene is known for its reactivity in electrophilic aromatic substitution reactions, which is a pivotal aspect in the synthesis of various derivatives.

Moreover, as a student of chemistry, it is essential to appreciate the broader implications of studying compounds like ethylsulfanylbenzene. As renowned chemist Robert H. Grubbs once said, "The beauty of chemistry is that it provides us the tools to uncover the secrets of the universe." Understanding such compounds contributes to that pursuit.

In summary, ethylsulfanylbenzene is not just a simple molecule; it opens the door to a vast array of scientific exploration and innovation.

Synonyms
Ethyl phenyl sulfide
622-38-8
(Ethylthio)benzene
UV3WD52QZX
Ethyl phenyl sulphide
EINECS 210-731-9
NSC-75124
AI3-17095
DTXSID60211236
DTXCID60133727
210-731-9
aehwkbxbxynpcx-uhfffaoysa-n
inchi=1/c8h10s/c1-2-9-8-6-4-3-5-7-8/h3-7h,2h2,1h
Benzene, (ethylthio)-
ethylsulfanylbenzene
Thiophenetole
Phenyl ethyl sulfide
(Ethylsulfanyl)benzene
Sulfide, ethyl phenyl
(Phenylthio)ethane
ETHYLTHIOBENZENE
(1-Thiapropyl)benzene
MFCD00009265
NSC 75124
ethylphenylsulfide
phenylethyl sulfide
ethylphenyl sulfide
ethy lphenyl sulfide
(Ethylsulfanyl)benzene #
UNII-UV3WD52QZX
Ethyl phenyl sulfide, 97%
SCHEMBL95992
NSC75124
AKOS006223893
GS-6872
Phenyl ethyl sulfide;Ethyl phenyl sulfide
DB-054101
E0426
NS00034972
H10383
Q27451730
F0001-1660
16M