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2,2-dimethyl-1,3-oxathiolane

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Identification
Molecular formula
C5H10OS
CAS number
693-75-8
IUPAC name
2,2-dimethyl-1,3-oxathiolane
State
State

At room temperature, 2,2-dimethyl-1,3-oxathiolane is in a liquid state.

Melting point (Celsius)
-56.00
Melting point (Kelvin)
217.15
Boiling point (Celsius)
141.00
Boiling point (Kelvin)
414.15
General information
Molecular weight
118.20g/mol
Molar mass
118.2030g/mol
Density
1.0470g/cm3
Appearence

2,2-Dimethyl-1,3-oxathiolane is a colorless to pale yellow liquid. It has a distinctive odor that can be reminiscent of sulfur or thiol compounds.

Comment on solubility

Solubility of 2,2-dimethyl-1,3-oxathiolane

2,2-dimethyl-1,3-oxathiolane, a five-membered ring compound, exhibits unique solubility characteristics that are influenced by its molecular structure. Understanding these properties is crucial for its applications in various chemical processes.

Key Solubility Features:

  • Polarity: The presence of the sulfur atom in the ring contributes to the overall polarity of the compound, which can enhance its solubility in polar solvents.
  • Solvent Compatibility: 2,2-dimethyl-1,3-oxathiolane is typically soluble in organic solvents such as ethanol, acetonitrile, and methanol, but may have limited solubility in non-polar solvents.
  • Influence of Temperature: As with many organic compounds, an increase in temperature can improve solubility, allowing adjustments in formulation and application.

In summary, the solubility of 2,2-dimethyl-1,3-oxathiolane is greatly dependent on polarity, the type of solvent used, and temperature. Therefore, it is important to carefully consider these factors for effective utilization in chemical reactions and processes.

Interesting facts

Interesting Facts about 2,2-Dimethyl-1,3-oxathiolane

2,2-Dimethyl-1,3-oxathiolane is a fascinating compound, particularly due to its unique structural characteristics and potential applications. Here are some intriguing aspects of this compound:

  • Structural Composition: This compound features a five-membered ring that includes both sulfur and oxygen atoms. This heterocyclic nature imparts distinct chemical properties compared to its saturated hydrocarbon counterparts.
  • Chemical Versatility: The presence of both dimethyl substitutions and a thiolane ring makes this compound a valuable intermediate in organic synthesis. This capability to undergo a variety of chemical reactions means it can serve as a building block to create more complex molecules.
  • Potential Applications: Due to its structure, 2,2-dimethyl-1,3-oxathiolane may find use in drug development and chemical manufacturing. Its ability to introduce a thiolane unit could be useful in medicinal chemistry for designing novel therapeutic agents.
  • Research Significance: The compound has been the subject of various studies focusing on its chemical reactivity and potential biological activities. Research indicates that compounds with similar structures often show enhanced activity against certain diseases.
  • Historical Context: Like many heterocycles, oxathiolanes have been of interest to chemists since the 20th century. The exploration of their properties has contributed significantly to the development of synthetic methodologies.

As science continues to advance, compounds like 2,2-dimethyl-1,3-oxathiolane represent a promising frontier in both research and industry, paving the way for innovative applications and discoveries.

Synonyms
2,2-Dimethyl-1,3-oxathiolane
1,3-OXATHIOLANE, 2,2-DIMETHYL-
5684-31-1
NSC 203379
BRN 0102790
I3E25G1WO7
NSC-203379
UNII-I3E25G1WO7
DTXSID20205373
5-19-01-00062 (Beilstein Handbook Reference)
DTXCID20127864
xlsczccjpdtcgu-uhfffaoysa-n
2,3-oxathiolane
NSC203379
SCHEMBL7382291
WLN: T5O CS BHJ B1 B1