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2-Phenyl-1,3-dithiolane

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Identification
Molecular formula
C9H10S2
CAS number
2227-32-7
IUPAC name
2-phenyl-1,3-dithiolane
State
State

At room temperature, 2-phenyl-1,3-dithiolane exists as a liquid. It is not very volatile under standard environmental conditions but should be handled with care due to its potential reactivity typical of organosulfur compounds.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
115.00
Boiling point (Kelvin)
388.15
General information
Molecular weight
170.29g/mol
Molar mass
170.2690g/mol
Density
1.1910g/cm3
Appearence

2-Phenyl-1,3-dithiolane is typically a colorless to pale yellow liquid. It is an organosulfur compound characterized by its distinctive dithiolane ring fused with a phenyl group, which imparts it a specific aromatic odor.

Comment on solubility

Solubility of 2-phenyl-1,3-dithiolane

2-phenyl-1,3-dithiolane is an interesting compound that showcases unique solubility characteristics.


When discussing the solubility of 2-phenyl-1,3-dithiolane, several key points come to mind:


  • Polar vs Nonpolar: Due to its structure, 2-phenyl-1,3-dithiolane is generally considered nonpolar, which influences its solubility in various solvents.
  • Solvent Compatibility: This compound tends to be soluble in nonpolar organic solvents, such as:
    • Benzene
    • Toluene
    • Chloroform
  • Water Solubility: Conversely, 2-phenyl-1,3-dithiolane is practically insoluble in water due to the inability of its nonpolar structure to interact favorably with polar water molecules.
  • Applications: Understanding its solubility properties is crucial for applications in organic synthesis and pharmaceuticals, where solvent choice can significantly impact reaction outcomes.

In summary, the solubility of 2-phenyl-1,3-dithiolane is primarily in nonpolar solvents, making it essential to consider solvent choice in practical applications. The understanding of such solubility characteristics can greatly enhance its utility in various chemical processes.

Interesting facts

Interesting Facts about 2-phenyl-1,3-dithiolane

2-phenyl-1,3-dithiolane is a fascinating compound that offers a glimpse into the world of organosulfur chemistry. Here are some intriguing aspects of this compound:

  • Structural Uniqueness: The 1,3-dithiolane ring structure not only gives this compound its name but also contributes to its chemical reactivity and stability. The presence of sulfur atoms makes the dithiolanes particularly interesting for various chemical transformations.
  • Versatile Reactivity: 2-phenyl-1,3-dithiolane can participate in a range of reactions, including nucleophilic substitutions and electrophilic additions, making it a useful building block in organic synthesis.
  • Application in Synthesis: Compounds like 2-phenyl-1,3-dithiolane are often used in the preparation of catalysts and can serve as intermediates in the synthesis of pharmaceuticals and agrochemicals.
  • Importance in Material Science: The properties of dithiolanes, including their ability to form stable organosulfur compounds, make them valuable in the development of new materials and polymers.
  • Biological Relevance: Some studies suggest that compounds containing dithiolane rings may exhibit biological activity, further expanding their potential applications in medicinal chemistry.

The study of 2-phenyl-1,3-dithiolane exemplifies how a simple structure can have profound implications in both academic research and practical applications. As with many chemical compounds, ongoing research continues to unveil new possibilities and uses for dithiolane derivatives.

Synonyms
2-Phenyl-1,3-dithiolane
5616-55-7
1,3-DITHIOLANE, 2-PHENYL-
Benzaldehyde ethylene dithioacetal
2-phenyl-[1,3]dithiolane
6FVQ28Z7PB
NSC-41541
NSC 41541
BRN 0120833
1,3-Dithiolan-2-yl, 2-phenyl-
NSC41541
MFCD01729637
UNII-6FVQ28Z7PB
SCHEMBL3078602
RKBPDPLCHXWHRQ-UHFFFAOYSA-
DTXSID30204695
RKBPDPLCHXWHRQ-UHFFFAOYSA-N
DTXSID601307760
AKOS006344767
72256-99-6
AS-38243
CS-0171315
P2742
InChI=1/C9H10S2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-5,9H,6-7H2