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1,3-Dithiolan-4-ylmethanol

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Identification
Molecular formula
C4H8OS2
CAS number
71463-29-1
IUPAC name
1,3-dithiolan-4-ylmethanol
State
State

At room temperature, 1,3-Dithiolan-4-ylmethanol is typically in a liquid state.

Melting point (Celsius)
-45.40
Melting point (Kelvin)
227.75
Boiling point (Celsius)
210.50
Boiling point (Kelvin)
483.65
General information
Molecular weight
136.22g/mol
Molar mass
136.2220g/mol
Density
1.2450g/cm3
Appearence

1,3-Dithiolan-4-ylmethanol appears as a colorless to pale yellow liquid. It may have a distinctive sulfide odor associated with sulfur-containing compounds.

Comment on solubility

Solubility of 1,3-Dithiolan-4-ylmethanol

1,3-Dithiolan-4-ylmethanol, a unique organosulfur compound, presents interesting solubility characteristics. Understanding the solubility of this compound can help in its applications and reactivity. Here are some key points to consider:

  • Polarity: Given its structure, 1,3-dithiolan-4-ylmethanol is likely to exhibit polar characteristics due to the presence of hydroxyl (-OH) and sulfur (-S-) groups, which can enhance its solubility in polar solvents.
  • Solvent Compatibility: This compound is expected to be soluble in water and other polar solvents like alcohols. However, it may have limited solubility in non-polar solvents such as hexane or benzene.
  • Hydrogen Bonding: The hydroxyl group can engage in hydrogen bonding with water molecules, further contributing to its solubility in aqueous environments.

In practical terms, solubility can be expressed as follows:

  • High solubility
  • Low solubility

As one dives deeper into the characteristics of 1,3-dithiolan-4-ylmethanol, it becomes clear that its solubility plays a pivotal role in determining its behavior in various chemical reactions and applications. Understanding these principles is crucial for chemists working with this compound.

Interesting facts

Interesting Facts about 1,3-Dithiolan-4-ylmethanol

1,3-Dithiolan-4-ylmethanol is a fascinating compound that belongs to the family of dithiolanes. This compound is characterized by the presence of both sulfur and carbon atoms, resulting in unique properties and reactivity. Below are some captivating aspects of this compound:

  • Structural Intricacies: The structure of 1,3-dithiolan-4-ylmethanol features a five-membered ring containing two sulfur atoms. This proximity of sulfur atoms often confers nucleophilic character to the compound, making it an intriguing candidate in organic synthesis.
  • Synthesizing Opportunities: Due to its structural features, the compound has potential applications in synthesizing other valuable chemical products. It can serve as a building block for creating larger molecules or complex organic compounds, which are pivotal in pharmaceuticals and materials science.
  • Biological Activities: Some derivatives of dithiolan compounds have shown interesting biological activities, including antimicrobial and antioxidant properties. This aspect opens avenues for research into the potential therapeutic uses of 1,3-dithiolan-4-ylmethanol and its analogs.
  • Flavor and Fragrance: Similar compounds within the dithiolane family are often explored for their unique flavor profiles. While not the primary focus for 1,3-dithiolan-4-ylmethanol, it is worth noting that certain dithiolanes can contribute to the aroma of certain foods, possibly making this compound useful in the food industry.

As research into this compound continues, we may uncover even more exciting applications and properties that contribute to the vast world of organic chemistry. The interplay of sulfur’s reactivity with carbon chains presents a rich field of study for chemists eager to explore the depths of molecular interactions.

Synonyms
1,3-DITHIOLANE-4-METHANOL
5862-51-1
BRN 1304599
5-19-02-00343 (Beilstein Handbook Reference)
SCHEMBL1860634
(1,3-Dithiolan-4-yl)methanol
4-hydroxymethyl-1,3-dithiolane
DTXSID60974157
NJXOBTJELQJDER-UHFFFAOYSA-N