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2-Ethyl-2-phenyl-1,3-dithiolane

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Identification
Molecular formula
C11H14S2
CAS number
18801-14-2
IUPAC name
2-ethyl-2-phenyl-1,3-dithiolane
State
State

At room temperature, 2-Ethyl-2-phenyl-1,3-dithiolane is found in a liquid state, which can vary in viscosity and color depending on its purity and environmental conditions.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
210.35g/mol
Molar mass
210.3440g/mol
Density
1.1600g/cm3
Appearence

2-Ethyl-2-phenyl-1,3-dithiolane is typically a colorless to pale yellow liquid. It may possess a distinctive odor characteristic of organosulfur compounds.

Comment on solubility

Solubility of 2-ethyl-2-phenyl-1,3-dithiolane

When discussing the solubility of 2-ethyl-2-phenyl-1,3-dithiolane, it's important to consider various factors that influence its behavior in different solvents. This compound, known for its unique structure, presents interesting solubility characteristics:

  • Polarity: The solubility is greatly affected by the polarity of solvents. 2-ethyl-2-phenyl-1,3-dithiolane is relatively non-polar due to its hydrocarbon-like structure, suggesting greater solubility in non-polar solvents such as hexane or toluene.
  • Temperature: Solubility is often temperature-dependent, with increased temperatures typically enhancing the solubility of many organic compounds.
  • Concentration: In concentrated solutions, interactions between molecules can reduce solubility, so it is essential to consider concentration when assessing solubility limits.
  • Functional Groups: The presence of sulfur atoms may provide a degree of compatibility with polar protic solvents, though overall solubility may still lean towards non-polar environments.

In summary, while the solubility of 2-ethyl-2-phenyl-1,3-dithiolane in water is expected to be low due to its non-polar nature, it holds promise for good solubility in non-polar organic solvents. Understanding these factors is pivotal for applications in chemical synthesis and industrial processes.

Interesting facts

Intriguing Facts about 2-Ethyl-2-phenyl-1,3-dithiolane

2-Ethyl-2-phenyl-1,3-dithiolane is an organosulfur compound that showcases some unique properties and applications:

  • Chemical Structure: This compound features a dithiolane core, which consists of a five-membered ring with two sulfur atoms. This structure contributes to its interesting chemical reactivity and stability compared to other thiol-derived compounds.
  • Flavor and Fragrance: Dithiolanes, including this one, are known for their potential use in the flavor and fragrance industry. Compounds containing sulfur can contribute to specific aromas and tastes that are distinctively recognized.
  • Synthetic Applications: 2-Ethyl-2-phenyl-1,3-dithiolane serves as a valuable intermediate in organic synthesis. The ability to modify its structure makes it a versatile building block in the development of complex organic molecules.
  • Biological Relevance: Sulfur-containing compounds like this one can exhibit interesting biological activity. Researchers are investigating the potential roles of such molecules in medicinal chemistry and their effects on biological systems.
  • Research Interest: As scientists delve deeper into the properties of organosulfur compounds, 2-ethyl-2-phenyl-1,3-dithiolane represents an exciting area of research. The insights gained from studying this compound may lead to the development of new materials or pharmaceuticals.

Overall, 2-ethyl-2-phenyl-1,3-dithiolane is not just a chemical abstract but a compound with practical implications and a vibrant profile in the realm of chemistry.

Synonyms
2-Ethyl-2-phenyl-1,3-dithiolane
BRN 0133372
1,3-DITHIOLANE, 2-ETHYL-2-PHENYL-
DTXSID60208823
4-19-00-00235 (Beilstein Handbook Reference)
DTXCID10131314
6008-82-8