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1,3-dithiane-4,5-diol

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Identification
Molecular formula
C4H8O2S2
CAS number
4612-65-5
IUPAC name
dithiane-4,5-diol
State
State

At room temperature, 1,3-dithiane-4,5-diol is in a solid state. The compound is stable under normal conditions and does not transition into other states of matter without the application of heat or other environmental changes.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.00
Boiling point (Celsius)
100.00
Boiling point (Kelvin)
373.00
General information
Molecular weight
138.21g/mol
Molar mass
138.2120g/mol
Density
1.5800g/cm3
Appearence

1,3-Dithiane-4,5-diol is typically found as a white or off-white crystalline solid. Its crystalline nature reflects its organized molecular structure, and the appearance can range from a fine powder to larger crystalline fragments.

Comment on solubility

Solubility of Dithiane-4,5-diol

Dithiane-4,5-diol is an interesting compound with notable solubility characteristics. Being a diol, it contains two hydroxyl groups (-OH) that can engage in hydrogen bonding, enhancing its interaction with polar solvents.

Here are some key points regarding its solubility:

  • Solvent Compatibility: Dithiane-4,5-diol is expected to be soluble in polar solvents such as water, due to its capability to form hydrogen bonds.
  • Solubility in Organic Solvents: It may also have some degree of solubility in less polar organic solvents, although this may vary depending on the specific solvent characteristics.
  • Temperature Dependence: Like many compounds, the solubility of dithiane-4,5-diol could increase with temperature, making it more soluble at elevated temperatures.

In summary, the solubility of dithiane-4,5-diol is influenced by its functional groups and the nature of the solvent used. This property can be utilized in various chemical applications, making it a compound of interest for further study.

Interesting facts

Interesting Facts about Dithiane-4,5-Diol

Dithiane-4,5-diol, a unique bifunctional compound, presents fascinating aspects of chemical reactivity and potential applications. Here are some key points of interest:

  • Structural Features: Dithiane-4,5-diol contains a six-membered ring with two sulfur atoms strategically positioned, offering both stability and reactivity.
  • Functional Versatility: The presence of hydroxyl groups makes this compound an excellent candidate for various chemical transformations. It can serve as a **nucleophile**, engaging in reactions that introduce further functional groups.
  • Role in Synthesis: Dithiane derivatives are often utilized in synthetic organic chemistry, providing an efficient pathway to create complex molecules. The ability of dithiane-4,5-diol to undergo redox reactions enhances its utility in synthetic schemes.
  • Biochemical Interest: Compounds with a dithiane structure have shown promise in medicinal chemistry. Their potential pharmacological activity is an area of ongoing research, contributing to the development of new therapeutic agents.
  • Educational Value: For chemistry students, studying dithiane-4,5-diol can provide insights into the reactivity of sulfur-containing compounds and broaden understanding of cyclic structures in organic synthesis.

As a compound that bridges theoretical knowledge and practical applications, dithiane-4,5-diol exemplifies the intriguing complexities present in the world of organic chemistry. It serves as a reminder of how even lesser-known compounds can play significant roles in advancing scientific understanding and technological innovation.

Synonyms
trans-4,5-dihydroxy-1,2-dithiacyclohexane
1,2-Dithiane-4,5-diol
trans-4,5-Dihydroxy-1,2-dithiane
dithiane-4,5-diol
14193-38-5
4,5-Dihydroxy-1,2-dithiane
EINECS 238-047-6
SCHEMBL561454
DTXSID20864661
YPGMOWHXEQDBBV-UHFFFAOYSA-N
NS00051953