1,2-Dithiolane
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| Names | |||
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| IUPAC name
1,2-Dithiolane | |||
| Identifiers | |||
3D model (JSmol) |
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| 102454 | |||
| ChEBI | |||
| ChemSpider | |||
| 1029938 | |||
PubChem CID |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| C3H6S2 | |||
| Molar mass | 106.20 g·mol−1 | ||
| Related compounds | |||
Related compounds |
Ethane-1,2-dithiol | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
1,2-Dithiolane is an organosulfur compound with the formula S2(CH2)3. It is also classified as a heterocycle derived from cyclopentane by replacing two methylene bridges (−CH2− units) with a disulfide group. 1,3-Dithiolane is an isomer. The parent molecule is unimportant but substituted derivatives, especially lipoic acid and its derivatives, are often essential for life. Several occur naturally.
The parent 1,2-dithiolane is the disulfide derived from 1,3-propanedithiol. It is however unstable with respect to oligomerization. In general, 1,3-dithiols are superior reductants relative to monothiols.