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2-Methyl-1,3-dithiolane

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Identification
Molecular formula
C4H8S2
CAS number
693-52-7
IUPAC name
2-methyl-1,3-dithiolane
State
State

At room temperature, 2-Methyl-1,3-dithiolane is in a liquid state, making it suitable for use in various chemical syntheses. It is stable under normal conditions but should be stored away from strong oxidizing agents.

Melting point (Celsius)
-88.00
Melting point (Kelvin)
185.15
Boiling point (Celsius)
145.00
Boiling point (Kelvin)
418.15
General information
Molecular weight
120.22g/mol
Molar mass
120.2170g/mol
Density
1.1209g/cm3
Appearence

The compound 2-Methyl-1,3-dithiolane is typically a clear to slightly yellow liquid. It has a distinctive odor reminiscent of sulfur compounds, which is characteristic of many dithiolane derivatives.

Comment on solubility

Solubility of 2-methyl-1,3-dithiolane

The compound 2-methyl-1,3-dithiolane, with its unique molecular structure, exhibits interesting solubility characteristics. It is important to note the following regarding its solubility:

  • Polarity: Due to the presence of sulfur atoms in its structure, 2-methyl-1,3-dithiolane has a somewhat polar character, which influences its solubility in various solvents.
  • Solvent Compatibility: This compound is generally soluble in polar organic solvents such as ethanol and methanol, but shows limited solubility in non-polar solvents like hexane or benzene.
  • Temperature Effects: Like many organic compounds, its solubility can increase with temperature—making it more soluble in warmer solvent systems.
  • Applications: The solubility of 2-methyl-1,3-dithiolane in certain solvents is valuable for its use in chemical reactions and synthesis, especially in biochemistry-related applications.

In summary, the solubility of 2-methyl-1,3-dithiolane is largely influenced by its molecular characteristics, making it essential to choose the right solvent for its effective use in various chemical processes. As a rule of thumb, like dissolves like, so opting for polar solvents may yield better solubility results.

Interesting facts

Interesting Facts About 2-Methyl-1,3-Dithiolane

2-Methyl-1,3-dithiolane, a five-membered ring compound, is a fascinating chemical with a variety of intriguing properties and applications. Here are some key points to consider:

  • Cyclic Structure: The presence of both sulfur atoms in a cyclic structure enhances the compound's uniqueness. The 2-methyl-1,3-dithiolane features a dithiolane ring that contributes to its distinct reactivity and stability compared to other sulfur-containing compounds.
  • Biochemical Relevance: This compound is particularly interesting in biochemistry and organic synthesis due to its potential as a reactive intermediate. It can be involved in various chemical reactions such as nucleophilic substitutions and electrophilic additions, making it useful for creating more complex molecules.
  • Odor and Flavor: Compounds with a similar sulfur structure often possess strong odors. In the case of 2-methyl-1,3-dithiolane, it has been noted to have a characteristic scent that could be linked to its potential use in food flavoring or fragrance formulations.
  • Synthesis: The synthetic pathways to create 2-methyl-1,3-dithiolane often involve straightforward methods, which may include condensation reactions of appropriate precursors. This accessibility makes it a sought-after building block for synthetic chemists.
  • Polymer Chemistry: This dithiolane can also play a role in polymer chemistry by serving as a cross-linking agent due to its ability to form stable bonds through its reactive sites. Its application in the development of novel materials highlights the compound's versatility.
  • Research Potential: The continuous exploration of compounds like 2-methyl-1,3-dithiolane can lead to significant advances in various fields, including medicinal chemistry, pharmaceuticals, and materials science. Its unique properties underscore the importance of sulfur-containing heterocycles in modern research.

In summary, 2-methyl-1,3-dithiolane is an excellent example of how simple organic molecules can have wide-ranging implications in both scientific research and practical applications. This compound continues to capture the interest of chemists across different disciplines!

Synonyms
2-Methyl-1,3-dithiolane
5616-51-3
1,3-DITHIOLANE, 2-METHYL-
2-Methyl-1,3-dithiacyclopentane
FEMA No. 3705
EINECS 227-038-2
UNII-4O81R0SPR0
NSC 227863
4O81R0SPR0
NSC-227863
DTXSID8063963
2-METHYL-1,3-DITHIOLANE [FHFI]
DTXCID6042028
227-038-2
carjcvdelamaej-uhfffaoysa-n
inchi=1/c4h8s2/c1-4-5-2-3-6-4/h4h,2-3h2,1h
MFCD01729666
NSC227863
SCHEMBL761708
Acetaldehdye ethylene thioacetal
FEMA 3705
2-Methyl-1,3-dithiolane, AldrichCPR
AKOS025396842
AS-81346
CS-0365126
NS00022383
F75650
Q27260281