Skip to main content

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

ADVERTISEMENT
Identification
Molecular formula
C10H12S2
CAS number
24722-10-9
IUPAC name
2-methyl-2-phenyl-1,3-dithiolane
State
State

At room temperature, 2-methyl-2-phenyl-1,3-dithiolane is typically found in a liquid state. The presence of sulfur atoms contributes to its unique characteristics compared to other hydrocarbons.

Melting point (Celsius)
24.00
Melting point (Kelvin)
297.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
194.34g/mol
Molar mass
194.3400g/mol
Density
1.1400g/cm3
Appearence

2-Methyl-2-phenyl-1,3-dithiolane is generally a colorless to pale yellow liquid. Due to the presence of the phenyl group, it emits a distinct aromatic smell, which is characteristic of compounds containing aromatic rings.

Comment on solubility

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

2-methyl-2-phenyl-1,3-dithiolane is an intriguing compound when it comes to its solubility characteristics. This compound has a unique structure that significantly influences how well it interacts with various solvents. Here are some key points to consider:

  • Solvent Polarity: The polar or nonpolar nature of the solvent plays a crucial role in the solubility of dithiolane derivatives. Since 2-methyl-2-phenyl-1,3-dithiolane contains multiple sulfur atoms, it tends to exhibit greater solubility in polar solvents such as dimethyl sulfoxide (DMSO) or ethanol.
  • Temperature Effects: As with many organic compounds, the solubility may increase with rising temperatures, making it more soluble in solvents at elevated temperatures.
  • Functional Group Influence: The presence of the dithiolane group provides unique interactivity with solvents, enhancing solubility in certain conditions.

It is essential to remember that factors influencing solubility could vary based on experimental conditions. Therefore, conducting thorough solubility tests under controlled environments yields a more accurate understanding of this compound's behavior in various solutions.

In summary, the solubility of 2-methyl-2-phenyl-1,3-dithiolane underscores a complex interplay of structural and environmental factors, making it a fascinating subject for further exploration.

Interesting facts

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

2-Methyl-2-phenyl-1,3-dithiolane is a fascinating compound that has caught the interest of chemists due to its unique structure and potential applications. Here are some intriguing insights into this compound:

  • Structural Uniqueness: The compound features a dithiolane ring, which consists of two sulfur atoms and a five-membered carbon ring. This unique architecture plays a crucial role in its reactivity.
  • Reactivity: Dithiolanes are known for their ability to participate in various chemical reactions, making them valuable intermediates in organic synthesis. Their reactivity stems from the presence of sulfur that can easily form bonds with other elements.
  • Applications: Compounds like 2-methyl-2-phenyl-1,3-dithiolane are often utilized in the synthesis of pharmaceuticals and agrochemicals. Their ability to serve as stabilizers or precursors in various formulations is noteworthy.
  • Chiral Centers: The presence of the methyl and phenyl groups introduces the possibility of chirality, which is a significant aspect in the field of asymmetric synthesis and drug development.
  • Biological Interest: Researchers have been investigating the biological activity of dithiolanes due to their potential as antioxidants and in various therapeutic applications.

In summary, 2-methyl-2-phenyl-1,3-dithiolane is a compound that presents a myriad of opportunities for exploration in both synthetic and medicinal chemistry. Its intriguing properties and applications reflect the underlying beauty of chemical research.

Synonyms
2-Methyl-2-phenyl-1,3-dithiolane
5769-02-8
1,3-DITHIOLANE, 2-METHYL-2-PHENYL-
NSC 218181
Y99X08O50E
2-Phenyl-2-methyl-1,3-dithiolane
NSC-218181
Acetophenone, cyclic ethylene mercaptole
NSC218181
UNII-Y99X08O50E
SCHEMBL11640241
NCOLUSQXCWLHEK-UHFFFAOYSA-
DTXSID80206386
2-methyl-2-phenyl-[1,3]dithiolane
Q27294404
InChI=1/C10H12S2/c1-10(11-7-8-12-10)9-5-3-2-4-6-9/h2-6H,7-8H2,1H3