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2-Isopropyl-1,3-oxathiolane

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Identification
Molecular formula
C6H12OS
CAS number
13693-12-0
IUPAC name
2-isopropyl-1,3-oxathiolane
State
State

The compound is usually in a liquid state at room temperature.

Melting point (Celsius)
-75.50
Melting point (Kelvin)
197.65
Boiling point (Celsius)
159.00
Boiling point (Kelvin)
432.15
General information
Molecular weight
132.23g/mol
Molar mass
132.2270g/mol
Density
0.9255g/cm3
Appearence

2-Isopropyl-1,3-oxathiolane is typically a colorless to pale yellow liquid. It may have a distinct, characteristic odor depending on its purity and concentration.

Comment on solubility

Solubility of 2-isopropyl-1,3-oxathiolane

2-isopropyl-1,3-oxathiolane is an intriguing compound with unique solubility characteristics. Understanding its solubility behavior is essential for various applications. Here are some key points to consider:

  • Polarity: The presence of the oxathiolane ring introduces some level of polarity to the compound, potentially influencing its solubility in polar solvents.
  • Solvent Compatibility: 2-isopropyl-1,3-oxathiolane tends to dissolve well in polar aprotic solvents like acetone or dimethyl sulfoxide (DMSO), but may have limited solubility in nonpolar solvents.
  • Temperature Effects: Like many organic compounds, solubility may vary with temperature; thus, higher temperatures could enhance solubility.
  • Concentration Considerations: At high concentrations, self-association may occur, which can affect the overall solubility profile.

To summarize, while 2-isopropyl-1,3-oxathiolane showcases interesting solubility properties, it primarily favors polar environments. Its behavior in various solvents can be crucial for practical applications in fields such as organic synthesis and pharmaceutical development.

Interesting facts

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

2-isopropyl-1,3-oxathiolane is a fascinating compound that showcases the intriguing world of cyclic sulfur compounds. Here are some noteworthy points about this compound:

  • Unique Structure: The oxathiolane ring incorporates both sulfur and oxygen in its cyclic framework, giving it unique chemical reactivity and properties that are often distinct from those of conventional hydrocarbons.
  • Synthetic Applications: This compound is of interest in chemical synthesis, particularly in the production of various pharmaceuticals and agrochemicals, where it may serve as an intermediate in multi-step reactions.
  • Use in Organic Chemistry: Its structure allows it to participate in various nucleophilic substitution reactions, making it a valuable compound for organic chemists seeking to develop new methods of synthesis.
  • Potential Biological Activity: Preliminary studies suggest that derivatives of 1,3-oxathiolanes may exhibit biological activities, potentially leading to the development of novel therapeutic agents.
  • Chiral Centers: 2-isopropyl-1,3-oxathiolane can also exhibit chirality, creating opportunities for the synthesis of enantiomerically pure compounds, which are crucial in the field of medicinal chemistry.

Overall, 2-isopropyl-1,3-oxathiolane serves as a key example of how structural diversity in chemistry can lead to innovative applications in various scientific fields. As research continues, this compound may reveal even more secrets that can be harnessed for future technologies and solutions.

Synonyms
2-Isopropyl-1,3-oxathiolane
2-propan-2-yl-1,3-oxathiolane
17643-70-8
2-Isopropyl-1,3-oxothiolane
BRN 0102812
1,3-OXATHIOLANE, 2-ISOPROPYL-
SCHEMBL11250642
DTXSID80938796
JTGZVABCBHZNLP-UHFFFAOYSA-N
2-(Propan-2-yl)-1,3-oxathiolane