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1,3-Propane sultone

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Identification
Molecular formula
C4H8O3S
CAS number
1120-71-4
IUPAC name
4-methyl-1,3,2-dioxathiane 2,2-dioxide
State
State

At room temperature, 1,3-Propane sultone is typically found as a solid. It has a relatively low melting point, transitioning to a liquid state just above ambient temperatures.

Melting point (Celsius)
31.00
Melting point (Kelvin)
304.15
Boiling point (Celsius)
148.00
Boiling point (Kelvin)
421.15
General information
Molecular weight
122.16g/mol
Molar mass
122.1580g/mol
Density
1.3370g/cm3
Appearence

1,3-Propane sultone is typically a white crystalline solid. It is known for its excellent ring stability and is used in a variety of chemical synthesis processes.

Comment on solubility

Solubility of 4-methyl-1,3,2-dioxathiane 2,2-dioxide

The solubility of 4-methyl-1,3,2-dioxathiane 2,2-dioxide is an intriguing topic, as its unique structure influences its interaction with solvents. In general, the solubility of a compound in a particular solvent can be affected by several factors, including the following:

  • Polarity: 4-methyl-1,3,2-dioxathiane 2,2-dioxide contains functional groups that may enhance its ability to dissolve in polar solvents such as water.
  • Temperature: Increased temperature often improves the solubility of organic compounds, potentially making this dioxathiane derivative more soluble at elevated temperatures.
  • Chain Length: The presence of the methyl group may affect the overall solubility by altering hydrophobic interactions.

Empirical studies suggest that this compound demonstrates moderate solubility in polar solvents due to its dioxathiane ring structure. For example, many researchers have noted, "polarity plays a crucial role in solvent interactions, determining the degree of solubility." It is important to highlight that, while it may dissolve well in specific solvents, its behavior in non-polar solvents is likely limited. Overall, understanding the solubility characteristics of 4-methyl-1,3,2-dioxathiane 2,2-dioxide is essential for its application in various chemical contexts.

Interesting facts

Interesting Facts About 4-Methyl-1,3,2-Dioxathiane 2,2-Dioxide

4-Methyl-1,3,2-dioxathiane 2,2-dioxide is a fascinating organic compound that belongs to the family of dioxathians. Here are some intriguing aspects about this unique compound:

  • Unique Structure: This compound features a six-membered ring containing two oxygen atoms and a sulfur atom, contributing to its distinct chemical properties. The presence of the dioxathiane ring is relatively rare, making it a subject of interest in chemical research.
  • Applications in Synthesis: 4-Methyl-1,3,2-dioxathiane 2,2-dioxide has garnered attention in synthetic organic chemistry. It can serve as a valuable precursor in synthesizing various pharmaceuticals and agrochemicals, demonstrating its practical importance in industrial applications.
  • Reactivity: The structure of this compound allows for unique reactivity pathways, particularly due to the presence of both sulfur and oxygen in the ring. This makes it an ideal candidate for further chemical transformations and modifications.
  • Research Interest: The compound is explored in the context of material science and catalysis. Ongoing research investigates its potential use as a catalyst in various reactions, highlighting its versatility.
  • Environmental Impact: Like many sulfur-containing compounds, 4-methyl-1,3,2-dioxathiane 2,2-dioxide is studied for its potential environmental impact. Understanding its degradation pathways is crucial for assessing safety and sustainability in its applications.

In summary, the multifaceted characteristics of 4-methyl-1,3,2-dioxathiane 2,2-dioxide showcase the compound's significance in both theoretical and practical chemistry. As scientists continue to explore its properties and applications, this compound will likely remain a point of interest in future studies!

Synonyms
4-Methyl-1,3,2-dioxathiane 2,2-dioxide
4426-50-0
1,3-Butylene sulfate
1,3-BUTYLENESULFATE
1-Methyltrimethylene sulfate
1,3-BUTANEDIOL, CYCLIC SULFATE
BRN 1238505
1,3,2-Dioxathiane, 4-methyl-, 2,2-dioxide
3-01-00-02171 (Beilstein Handbook Reference)
SCHEMBL5989973
DTXSID70963198
KLXMOOWASHTDLR-UHFFFAOYSA-N
MFCD00142517
AKOS006274920
4-Methyl-1,3,2-dioxathiane2,2-dioxide
4-Methyl-[1,3,2]dioxathiane 2,2-dioxide
4-Methyl-1,3,2lambda~6~-dioxathiane-2,2-dione