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2-(2-phenylethyl)-1,3-dithiolane

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Identification
Molecular formula
C11H14S2
CAS number
35525-57-4
IUPAC name
2-(2-phenylethyl)-1,3-dithiolane
State
State

It is typically found as a liquid at room temperature, which contributes to its utility in various flavoring applications due to its volatility.

Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.15
Boiling point (Celsius)
261.00
Boiling point (Kelvin)
534.15
General information
Molecular weight
212.36g/mol
Molar mass
212.3600g/mol
Density
1.1690g/cm3
Appearence

The compound is a colorless to pale yellow liquid. It emits a distinctive odor that can be described as similar to natural truffle or garlic-like aromas.

Comment on solubility

Solubility of 2-(2-phenylethyl)-1,3-dithiolane

The solubility of 2-(2-phenylethyl)-1,3-dithiolane can be described as relatively low in polar solvents but may exhibit moderate solubility in non-polar or organic solvents. This solubility behavior can be attributed to its unique molecular structure which includes:

  • Non-polar characteristics: The presence of aromatic rings typically indicates a tendency to interact favorably with non-polar solvents.
  • Sulfur atoms: The dithiolane feature can engage in weak dipole interactions, which may contribute to selective solubility.

Due to these factors, when assessing its capacity to dissolve, consider:

  1. Solvent type: Best results may be obtained in solvents such as dichloromethane or ethyl acetate.
  2. Temperature influence: Enhanced temperatures could potentially increase solubility due to improved molecular motion.

In summary, while 2-(2-phenylethyl)-1,3-dithiolane may not be readily soluble in water, it finds better compatibility in organic media. This characteristic highlights the importance of choosing the right solvent for effective dissolution,
allowing for better utilization in chemical and pharmaceutical applications.

Interesting facts

Interesting Facts about 2-(2-phenylethyl)-1,3-dithiolane

2-(2-phenylethyl)-1,3-dithiolane is a fascinating organic compound that falls under the category of dithiolanes. This compound has drawn considerable interest due to its unique structural features and potential applications. Here are some intriguing aspects to consider:

  • Structural Complexity: The compound contains a dithiolane ring, which features two sulfur atoms in a five-membered ring structure. This contributes to the compound's distinctive chemical properties.
  • Functional Groups: The presence of the 2-phenylethyl substituent contributes aromatic characteristics, which can influence its reactivity and interaction with other molecules.
  • Potential Applications: Compounds like 2-(2-phenylethyl)-1,3-dithiolane are being explored in fields such as organic synthesis, medicinal chemistry, and materials science. Their unique properties can make them candidates for new drug formulations or innovative materials.
  • Reactivity: The sulfur atoms in the dithiolane structure can participate in various chemical reactions, including oxidation and nucleophilic attacks, making this compound interesting for synthetic chemists.

In the words of a prominent chemist, "The beauty of organic chemistry lies in its myriad of structures and the interactions they facilitate." This statement resonates particularly with compounds like 2-(2-phenylethyl)-1,3-dithiolane, where structural intricacies pave the way for exciting research and discovery.


Overall, 2-(2-phenylethyl)-1,3-dithiolane serves as a reminder of the incredible diversity and potential within the realm of organic compounds. Its structural uniqueness and varied applications make it a worthy subject of study in the field of chemistry.

Synonyms
1,3-DITHIOLANE, 2-PHENETHYL-
14505-46-5
2-Phenethyl-1,3-dithiolane
BRN 1307551
SCHEMBL4258932
SCHEMBL4258936
DTXSID40162873