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2-Ethyl-2-methyl-1,3-dithiolane

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Identification
Molecular formula
C6H12S2
CAS number
19417-13-5
IUPAC name
2-ethyl-2-methyl-1,3-dithiolane
State
State

At room temperature, 2-Ethyl-2-methyl-1,3-dithiolane is a liquid. Its low melting point ensures it remains in the liquid state under standard conditions.

Melting point (Celsius)
-42.00
Melting point (Kelvin)
231.15
Boiling point (Celsius)
153.00
Boiling point (Kelvin)
426.15
General information
Molecular weight
148.29g/mol
Molar mass
148.2900g/mol
Density
1.0590g/cm3
Appearence

2-Ethyl-2-methyl-1,3-dithiolane typically appears as a colorless liquid. It may possess a sulfurous or onion-like odor characteristic of many organosulfur compounds. Due care must be taken while handling to avoid inhalation or prolonged exposure.

Comment on solubility

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

The solubility of 2-ethyl-2-methyl-1,3-dithiolane is an interesting characteristic that can greatly influence its applications in various chemical processes. Here are some key points to consider:

  • Polar vs Non-Polar Solubility: This compound is categorized as a non-polar solvent, which typically results in low solubility in polar solvents like water.
  • Solubility in Organic Solvents: However, 2-ethyl-2-methyl-1,3-dithiolane demonstrates good solubility in organic solvents such as hexane, ethyl acetate, and other hydrocarbons.
  • Temperature Impact: Solubility may also be affected by temperature changes; generally, increasing temperature can enhance the solubility in organic solvents.

In consideration of these factors, it is often found that the predictive solubility behavior is aligned with the principle of "like dissolves like." Therefore, for effective utilization or handling of 2-ethyl-2-methyl-1,3-dithiolane, one should always consult relevant solubility tables or conduct empirical testing to ensure compatibility with chosen solvents.

Interesting facts

Interesting Facts about 2-ethyl-2-methyl-1,3-dithiolane

2-ethyl-2-methyl-1,3-dithiolane is a fascinating compound that stands out due to its unique structure and potential applications. Here are some captivating aspects of this compound:

  • Structural Characteristics: This compound is notable for its dithiolane ring, which features two sulfur atoms. This heterocyclic nature contributes to its distinct chemical reactivity and properties.
  • Applications in Chemistry: Due to its reactive sulfide groups, 2-ethyl-2-methyl-1,3-dithiolane plays roles in various organic synthesis reactions. It can serve as a building block in the production of more complex molecules, particularly in creating sulfur-containing compounds.
  • Role in Flavor Chemistry: The compound is also of interest in the field of flavor chemistry. Its unique structure may contribute to its potential as a flavoring agent, providing distinct notes that enhance the sensory profile of food products.
  • Research Potential: Ongoing research into dithiolane derivatives like 2-ethyl-2-methyl-1,3-dithiolane can unveil new chemical behaviors that may be useful in materials science, pharmaceuticals, and nanotechnology.

In summary, the intriguing nature of 2-ethyl-2-methyl-1,3-dithiolane lies in its structural properties and diverse applications. As quoted by many researchers in the field, "The simple nature of these compounds often belies their potential for complex applications." Exploring compounds like this one allows chemists to uncover innovative solutions in various industries.

Synonyms
2-Ethyl-2-methyl-1,3-dithiolane
1,3-DITHIOLANE, 2-ETHYL-2-METHYL-
BRN 0102819
DTXSID00208822
2-Methyl-2-ethyl-1,3-dithiolane
4-19-00-00069 (Beilstein Handbook Reference)
DTXCID50131313
htkivhyynmkzdn-uhfffaoysa-n
6008-81-7
SCHEMBL5086639
STL563406
AKOS024336467