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Ethyl Vinyl Sulfide

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Identification
Molecular formula
C4H8S
CAS number
137-07-5
IUPAC name
vinylsulfanylethane
State
State

At room temperature, Ethyl Vinyl Sulfide exists as a liquid.

Melting point (Celsius)
-137.00
Melting point (Kelvin)
136.15
Boiling point (Celsius)
86.00
Boiling point (Kelvin)
359.15
General information
Molecular weight
88.17g/mol
Molar mass
88.1710g/mol
Density
0.9610g/cm3
Appearence

Ethyl Vinyl Sulfide is a colorless to pale yellow liquid.

Comment on solubility

Solubility of Vinylsulfanylethane

Vinylsulfanylethane, with the chemical formula C4H6S, exhibits some interesting solubility characteristics. Understanding the solubility of this compound can be essential in various application contexts. Here are some key points to consider:

  • Polarity: Vinylsulfanylethane features a polar vinylsulfanyl group, suggesting it could interact favorably with polar solvents.
  • Solvent Compatibility: It is generally expected to be soluble in organic solvents such as:
    • Alcohols
    • Acetone
    • Dichloromethane
  • Aqueous Solubility: The compound is likely to exhibit low solubility in water due to its hydrophobic ethane backbone.
  • Concentration Effects: Like many organic compounds, its solubility can also be affected by temperature and the concentration of the solvent.

In summary, while vinylsulfanylethane shows promise for solubility in certain organic solvents, it is less likely to dissolve well in water. This has important implications for its use in chemical synthesis and other practical applications. As a general rule, one might say, "Select your solvent wisely to maximize solubility!"

Interesting facts

Interesting Facts about Vinylsulfanylethane

Vinylsulfanylethane, an intriguing organosulfur compound, holds a unique place in chemical studies due to its structure and potential applications. Here are some fascinating aspects:

  • Structure: Vinylsulfanylethane features a vinyl group attached to a sulfur atom, which contributes to its reactivity in various chemical reactions. This molecular configuration allows for interesting interactions with other compounds.
  • Reactant in Synthesis: This compound is often used as a reagent in organic synthesis, particularly in the formation of sulfoxides and sulfones, expanding its utility in creating more complex molecular frameworks.
  • Role in Materials Science: Vinylsulfanylethane may play a role in developing new materials, especially in polymer science, where the incorporation of sulfur can lead to enhanced thermal stability and chemical resistance.
  • Flavors and Fragrances: Compounds like vinylsulfanylethane can be utilized in the industry to create specific flavors and fragrances. The distinctive scent profile emerging from sulfur compounds can contribute to desirable qualities in consumer products.
  • Research Interest: The intriguing reactions of vinylsulfanylethane have caught the attention of chemists looking to explore new ways to harness sulfur chemistry, which has implications ranging from pharmaceuticals to agricultural chemicals.

As a compound that bridges several fields of study, vinylsulfanylethane is a testament to the beauty of chemistry, providing multiple avenues for exploration and innovation.

Synonyms
Ethyl vinyl sulfide
627-50-9
(Ethylthio)ethene
Ethylvinyl sulfide
CH2=CHSC2H5
vinyl ethyl sulfide
5PXS818N9W
ETHYLSULFANYLETHENE
NSC 90866
NSC-90866
UNII-5PXS818N9W
DTXSID50211765
DTXCID80134256
625-942-5
afgacprtzocniw-uhfffaoysa-n
inchi=1/c4h8s/c1-3-5-4-2/h3h,1,4h2,2h
ethenylsulfanylethane
Ethene, (ethylthio)-
Vinyl ethyl thioether
SULFIDE, ETHYL VINYL
ethyl(vinyl)sulfane
(ethylsulfanyl)ethene
MFCD00015180
Ethyl vinyl sulfide, 96%
1-(Ethylsulfanyl)ethylene #
WLN: 2S1U1
NSC90866
AKOS015915446
E0335
D90486