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4-Methyl-2-phenyl-1,3-dithiolane

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Identification
Molecular formula
C10H12S2
CAS number
5737-03-1
IUPAC name
4-methyl-2-phenyl-1,3-dithiolane
State
State

At room temperature, 4-methyl-2-phenyl-1,3-dithiolane exists in a liquid state. Its volatility and odor are characteristic of many sulfide compounds.

Melting point (Celsius)
-57.00
Melting point (Kelvin)
216.15
Boiling point (Celsius)
125.00
Boiling point (Kelvin)
398.15
General information
Molecular weight
196.32g/mol
Molar mass
196.3200g/mol
Density
1.1350g/cm3
Appearence

4-Methyl-2-phenyl-1,3-dithiolane is typically a colorless to pale yellow liquid when pure. It may appear as a more amber color if impurities are present. It is an organic compound with a notable sulfide-like odor due to the presence of sulfur atoms in the dithiolane ring.

Comment on solubility

Solubility of 4-methyl-2-phenyl-1,3-dithiolane

The solubility of 4-methyl-2-phenyl-1,3-dithiolane can be described as intriguing and complex due to its unique molecular structure. This compound is primarily characterized as a heterocyclic compound that exhibits certain solubility behaviors:

  • Non-polar characteristics: The presence of the methyl and phenyl groups indicates that it is relatively non-polar.
  • Solvent interaction: 4-methyl-2-phenyl-1,3-dithiolane will likely show solubility in non-polar solvents such as:
    • Hexane
    • Ether
    • Chloroform
  • Limited solubility in water: Due to its non-polar nature and the lack of strong hydrogen bonding capabilities, it is expected to have poor solubility in polar solvents such as water.

In summary, the solubility of 4-methyl-2-phenyl-1,3-dithiolane can be characterized by its affinity for non-polar solvents while showing significant limitations in polar environments.

Interesting facts

Interesting Facts about 4-methyl-2-phenyl-1,3-dithiolane

4-methyl-2-phenyl-1,3-dithiolane is a fascinating compound that belongs to the class of dithiolanes, known for their unique ring structure. This compound is particularly interesting due to several key features:

  • Unique Structure: The presence of both sulfur atoms and a methyl and phenyl group in its structure gives it distinct chemical properties that make it a subject of study in organic chemistry.
  • Reactivity: Dithiolanes can participate in various chemical reactions, including nucleophilic attacks and cycloadditions, making them versatile intermediates for synthesizing other compounds.
  • Potential Applications: Compounds like 4-methyl-2-phenyl-1,3-dithiolane have potential applications in materials science, particularly in the development of new polymers and compounds that may exhibit specific electrical or optical properties.
  • Natural Occurrence: Interestingly, some dithiolanes and their derivatives have been found in natural products, suggesting that they may play roles in biological systems.

In the world of organic synthesis, chemists often say: "Dithiolane derivatives pave the way for complex molecular architectures." This quote captures the essence of the compound's significance in synthetic chemistry. As research continues, it is likely that 4-methyl-2-phenyl-1,3-dithiolane will unveil even more intriguing aspects of its chemistry, further expanding our understanding of dithiolane structures and their interactions.

Synonyms
4-Methyl-2-phenyl-1,3-dithiolane
BRN 5508179
1,3-DITHIOLANE, 4-METHYL-2-PHENYL-
DTXSID10971535
DTXCID601399046
5616-53-5
SCHEMBL10956530