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2-Phenyl-2-propyl-1,3-dithiolane

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Identification
Molecular formula
C12H16S2
CAS number
5907-38-0
IUPAC name
2-phenyl-2-propyl-1,3-dithiolane
State
State

At room temperature, 2-Phenyl-2-propyl-1,3-dithiolane is in a liquid state. It is not very volatile, making it stable under standard conditions of temperature and pressure.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
208.36g/mol
Molar mass
208.3610g/mol
Density
1.0900g/cm3
Appearence

2-Phenyl-2-propyl-1,3-dithiolane is typically a colorless to light yellow liquid with a distinct odor. It can appear oily and may darken when exposed to air or light.

Comment on solubility

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

2-phenyl-2-propyl-1,3-dithiolane, a member of the dithiolane family, displays some intriguing characteristics regarding its solubility. Generally, the solubility of organic compounds like this one is influenced by several factors:

  • Polarity: The presence of sulfur atoms and aromatic phenyl groups can affect the overall polarity of the compound.
  • Temperature: Solubility tends to increase with temperature for many organic substances; thus, elevating the temperature may enhance the solubility of 2-phenyl-2-propyl-1,3-dithiolane in organic solvents.
  • Solvent Type: This compound is expected to be more soluble in non-polar organic solvents due to its hydrophobic structure.

In general, while 2-phenyl-2-propyl-1,3-dithiolane may present limited solubility in water, it can exhibit reasonable solubility in organic solvents such as:

  1. Diethyl ether
  2. Toluene
  3. Chloroform

In summary, understanding the solubility of 2-phenyl-2-propyl-1,3-dithiolane requires a consideration of its molecular structure, solvent interactions, and environmental conditions. As with many organic compounds, *solubility is a complex interplay of these factors* that must be taken into account for practical applications.

Interesting facts

Interesting Facts About 2-phenyl-2-propyl-1,3-dithiolane

2-phenyl-2-propyl-1,3-dithiolane is a fascinating compound that belongs to the class of dithiolanes, characterized by having two sulfur atoms in its five-membered ring structure. Here are some intriguing aspects of this compound:

  • Cyclic Structure: The inclusion of sulfur atoms in the ring significantly influences the compound's reactivity and stability. The unique heterocyclic nature contributes to its notable chemical behavior.
  • Applications in Organic Synthesis: This compound serves as an essential intermediate in organic synthesis, particularly in the preparation of various sulfur-containing compounds, which are crucial in many industrial applications.
  • Potential Biological Activity: Research indicates that dithiolane derivatives may possess properties beneficial for biological applications, such as antioxidant activity. This characteristic is particularly interesting for pharmaceutical developments.
  • Synthetic Versatility: The ability of dithiolanes to undergo numerous chemical transformations opens up avenues for the creation of complex molecules, making them invaluable in medicinal chemistry.
  • Flavor and Aroma: Compounds like 2-phenyl-2-propyl-1,3-dithiolane might influence flavor and fragrance formulations, adding unique notes to various products.

In conclusion, 2-phenyl-2-propyl-1,3-dithiolane showcases a combination of chemical versatility and potential practical applications. Its structure and reactivity make it an essential compound in both academic research and industrial processes, reminding us of the endless possibilities within organic chemistry.

Synonyms
2-Phenyl-2-propyl-1,3-dithiolane
BRN 0147528
1,3-DITHIOLANE, 2-PHENYL-2-PROPYL-
5769-03-9
DTXSID40206387
4-19-00-00243 (Beilstein Handbook Reference)
DTXCID40128878