Potassium p-Toluenethiosulfonate
≥98%
- Product Code: 122586
CAS:
28519-50-8
| Molecular Weight: | 226.35 g./mol | Molecular Formula: | C₇H₇KO₂S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00003547 | |
| Melting Point: | 229°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Potassium p-Toluenethiosulfonate is widely used in organic synthesis as a versatile reagent. It is particularly effective in the preparation of thioethers and sulfides, which are important intermediates in the production of pharmaceuticals and agrochemicals. The compound is also employed in the synthesis of sulfur-containing heterocycles, which are valuable in medicinal chemistry for developing drugs with therapeutic properties. Additionally, it serves as a key component in the modification of peptides and proteins, enabling the introduction of thiol groups for further functionalization. Its role in cross-coupling reactions further enhances its utility in creating complex organic molecules.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 97.5-100 |
| Water | 5-9 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £26.91 |
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| 5.000 | 10-20 days | £119.42 |
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| 25.000 | 10-20 days | £390.14 |
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| 100.000 | 10-20 days | £1,153.47 |
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Potassium p-Toluenethiosulfonate
Potassium p-Toluenethiosulfonate is widely used in organic synthesis as a versatile reagent. It is particularly effective in the preparation of thioethers and sulfides, which are important intermediates in the production of pharmaceuticals and agrochemicals. The compound is also employed in the synthesis of sulfur-containing heterocycles, which are valuable in medicinal chemistry for developing drugs with therapeutic properties. Additionally, it serves as a key component in the modification of peptides and proteins, enabling the introduction of thiol groups for further functionalization. Its role in cross-coupling reactions further enhances its utility in creating complex organic molecules.
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