Tris(tert-butoxy)silanethiol
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| Names | |||
|---|---|---|---|
| IUPAC name
Tris(tert-butoxy)silanethiol | |||
| Other names
Tri(tert-butoxy)silanethiol | |||
| Identifiers | |||
| 690-52-8 | |||
| Abbreviations | TBST | ||
| ChemSpider | 4414610 | ||
| Jmol interactive 3D | Image | ||
| PubChem | 5246420 | ||
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| Properties | |||
| C12H28O3SSi | |||
| Molar mass | 280.50 g·mol−1 | ||
| Appearance | Colourless liquid | ||
| Boiling point | 113 to 115 °C (235 to 239 °F; 386 to 388 K) at 35 mmHg | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
| Infobox references | |||
Tris(tert-butoxy)silanethiol is a silicon compound containing three tert-butoxy groups and a rare Si-S-H functional group. This colourless compound serves as an hydrogen donor in radical chain reactions. It is prepared by alcoholysis of silicon disulfide and purified by distillation:
- 3 (CH3)3COH + SiS2 → [(CH3)3CO]3SiSH + H2S
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