Tris(ethylthio)methane
≥98%
- Product Code: 121811
CAS:
6267-24-9
| Molecular Weight: | 196.39 g./mol | Molecular Formula: | C₇H₁₆S₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00015179 | |
| Melting Point: | Boiling Point: | 80°C/0.4mmHg(lit.) | |
| Density: | Storage Condition: | room temperature |
Product Description:
Tris(ethylthio)methane is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. It serves as a key reagent in the preparation of sulfur-containing compounds, which are often employed in the development of pharmaceuticals and agrochemicals. Its unique structure allows it to act as a precursor in the synthesis of thioethers and other sulfur-based derivatives, which are valuable in medicinal chemistry for their bioactivity. Additionally, it is used in material science for the development of sulfur-rich polymers and coatings, offering enhanced durability and resistance to degradation. The compound's ability to form stable intermediates also makes it useful in catalytic processes and cross-coupling reactions, contributing to advancements in synthetic methodologies.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Yellow To Green Clear Liquid |
| Purity (%) | 98 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,620.00 |
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Tris(ethylthio)methane
Tris(ethylthio)methane is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. It serves as a key reagent in the preparation of sulfur-containing compounds, which are often employed in the development of pharmaceuticals and agrochemicals. Its unique structure allows it to act as a precursor in the synthesis of thioethers and other sulfur-based derivatives, which are valuable in medicinal chemistry for their bioactivity. Additionally, it is used in material science for the development of sulfur-rich polymers and coatings, offering enhanced durability and resistance to degradation. The compound's ability to form stable intermediates also makes it useful in catalytic processes and cross-coupling reactions, contributing to advancements in synthetic methodologies.
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