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2-(p-Tolyl)-1,3-dithiolane

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Identification
Molecular formula
C10H12S2
CAS number
78865-71-3
IUPAC name
2-(p-tolyl)-1,3-dithiolane
State
State

At room temperature, 2-(p-Tolyl)-1,3-dithiolane is typically in a liquid state.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.15
General information
Molecular weight
196.32g/mol
Molar mass
196.3200g/mol
Density
1.1665g/cm3
Appearence

The compound 2-(p-Tolyl)-1,3-dithiolane usually appears as a clear, colorless to slightly yellow liquid. Its appearance may vary slightly depending on the purity of the sample.

Comment on solubility

Solubility of 2-(p-tolyl)-1,3-dithiolane

2-(p-tolyl)-1,3-dithiolane, with its unique structural characteristics, displays intriguing solubility properties that are important to its applications.

Solubility Characteristics:

  • Polar vs. Non-Polar Solvents: The presence of both the p-tolyl group and the dithiolane ring influences its solubility. Generally, compounds with significant non-polar character like 2-(p-tolyl)-1,3-dithiolane tend to be more soluble in non-polar solvents.
  • Common Solvents: This compound is often soluble in organic solvents such as ether, benzene, and chloroform, while showing limited solubility in polar solvents like water.
  • Temperature Effects: Variations in temperature can also affect the solubility. Typically, increasing the temperature enhances solubility for many organic compounds, including dithiolanes.

As noted, the solubility of 2-(p-tolyl)-1,3-dithiolane is primarily influenced by its molecular structure, which results in a preference for non-polar environments. In summary, this compound's solubility profile can be summarized as:

  1. Better solubility in non-polar solvents.
  2. Poor solubility in polar solvents.
  3. Potential increase in solubility with increased temperature.

Understanding these solubility properties is essential for utilizing this compound effectively in various chemical applications.

Interesting facts

Interesting Facts About 2-(p-Tolyl)-1,3-dithiolane

2-(p-Tolyl)-1,3-dithiolane is a fascinating compound that belongs to a class of chemicals known as dithiolanes, which are characterized by the presence of two sulfur atoms in a five-membered ring. This compound features intriguing properties and applications, making it a topic of interest for both chemists and students alike. Here are some noteworthy aspects of 2-(p-Tolyl)-1,3-dithiolane:

  • Structural Characteristics: The presence of a p-tolyl group enhances the molecular stability and hydrophobic characteristics of the compound, which can affect its reactivity.
  • Reactivity: Dithiolanes are known for their nucleophilic properties. This compound can engage in various reactions, allowing it to participate in complex synthesis processes.
  • Applications in Synthesis: 2-(p-Tolyl)-1,3-dithiolane is utilized in organic synthesis, particularly in the preparation of other valuable chemicals, including pharmaceuticals and agrochemicals.
  • Role in Organosulfur Chemistry: Compounds like this play a significant role in organosulfur chemistry, which is vital for developing new materials and understanding biological systems.
  • Biological Relevance: Research suggests that dithiolanes could have potential biological activities, including antimicrobial properties, thus opening avenues for medicinal chemistry research.

As the world of chemistry continues to evolve, understanding compounds like 2-(p-Tolyl)-1,3-dithiolane reveals the intricate relationships between structure and function. In the words of a renowned chemist, "Understanding the molecular intricacies of compounds is the key to unlocking their potential." The study of such compounds not only enriches our knowledge but also contributes to innovation in various fields.

Synonyms
2-(p-Tolyl)-1,3-dithiolane
23229-29-0
1,3-DITHIOLANE, 2-(p-TOLYL)-
2-(4'-Methylphenyl)-1,3-dithiolane
DTXSID40177801
BRN 0130878
2-(4-Methylphenyl)-1,3-dithiolane
1,3-Dithiolane, 2-p-tolyl-
1,3-Dithiolane, 2-(4-methylphenyl)-
RefChem:1061125
SCHEMBL5132106
DTXCID60100292
2-(4-Methylphenyl)-1,3-dithiolane #