Methyl4-mercaptobenzoate
95%
- Product Code: 64697
CAS:
6302-65-4
| Molecular Weight: | 168.22 g./mol | Molecular Formula: | C₈H₈O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863423 | |
| Melting Point: | 33-36 °C (lit.) | Boiling Point: | 266.7 °C at 760 mmHg (lit.) |
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
Methyl 4-mercaptobenzoate is widely used in organic synthesis as a building block for creating more complex molecules. Its thiol group makes it valuable for forming sulfur-containing compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the preparation of ligands for metal complexes, particularly in catalysis and material science. Additionally, this compound finds applications in the development of polymers and resins, where its reactivity can enhance material properties. In research, it serves as a reagent for studying thiol-ene reactions, which are important in click chemistry for creating diverse molecular structures.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Pale Yellow Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,980.00 |
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| 0.500 | 10-20 days | ฿9,900.00 |
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Methyl4-mercaptobenzoate
Methyl 4-mercaptobenzoate is widely used in organic synthesis as a building block for creating more complex molecules. Its thiol group makes it valuable for forming sulfur-containing compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the preparation of ligands for metal complexes, particularly in catalysis and material science. Additionally, this compound finds applications in the development of polymers and resins, where its reactivity can enhance material properties. In research, it serves as a reagent for studying thiol-ene reactions, which are important in click chemistry for creating diverse molecular structures.
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