1,3-dithiane-4,5-diol
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- Molecular formula
- C4H8O2S2
- CAS Number
- 4612-65-5
- IUPAC Name
- dithiane-4,5-diol
- Molecular Weight
- 138.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5800g/cm3
- Appearance
- can range from a fine powder to larger crystalline fragments.
- Synonyms
- trans-4, 5-dihydroxy-1, 2-dithiacyclohexane
Identification
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.