4-Acetamidothiophenol
95%
- Product Code: 118845
Alias:
4-Acetaminothiophenol; p-Acetaminothiophenol
CAS:
1126-81-4
| Molecular Weight: | 167.23 g./mol | Molecular Formula: | C₈H₉NOS |
|---|---|---|---|
| EC Number: | 214-427-7 | MDL Number: | MFCD00004848 |
| Melting Point: | 150-153 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its thiol group allows for the formation of disulfide bonds, making it valuable in the development of peptide-based drugs and other bioactive molecules. Additionally, it finds application in the preparation of specialty polymers and resins, where it acts as a cross-linking agent or modifier to enhance material properties. In research, it is utilized for studying thiol-disulfide exchange reactions, which are critical in understanding redox processes in biological systems. Its role in synthesizing sulfur-containing compounds also extends to the creation of ligands for metal catalysis in industrial chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 150-157 |
| Purity (Titration) | 95-100 |
| Appearance | Yellow Powder Crystals And/Or Chunks |
| Infrared Spectrum | Conforms To Structure |
| Solubility In Meoh | Colorless To Yellow, Clear, 25Mg/Ml |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿750.00 |
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| 5.000 | 10-20 days | ฿2,000.00 |
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4-Acetamidothiophenol
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its thiol group allows for the formation of disulfide bonds, making it valuable in the development of peptide-based drugs and other bioactive molecules. Additionally, it finds application in the preparation of specialty polymers and resins, where it acts as a cross-linking agent or modifier to enhance material properties. In research, it is utilized for studying thiol-disulfide exchange reactions, which are critical in understanding redox processes in biological systems. Its role in synthesizing sulfur-containing compounds also extends to the creation of ligands for metal catalysis in industrial chemical processes.
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