2,3,5,6-Tetrafluoro-4-mercaptobenzoic Acid
≥98%
- Product Code: 94055
CAS:
5211-44-9
| Molecular Weight: | 226.14 g./mol | Molecular Formula: | C₇H₂F₄O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 151-155°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
2,3,5,6-Tetrafluoro-4-mercaptobenzoic Acid is primarily used in the field of organic synthesis and material science. Its unique structure, featuring both thiol and carboxylic acid functional groups, makes it a valuable building block for creating complex molecules. It is often employed in the development of advanced polymers and coatings, where its fluorine atoms contribute to enhanced chemical resistance and durability. Additionally, this compound is utilized in the synthesis of pharmaceuticals and agrochemicals, where its reactive sites allow for precise modifications to achieve desired biological activities. In research, it serves as a key intermediate for studying thiol-based reactions and fluorine chemistry, aiding in the discovery of new materials and compounds with specialized properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white to Light yellow to Light orange powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| MELTING POINT | 151-155 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,290.00 |
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| 1.000 | 10-20 days | ฿8,990.00 |
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2,3,5,6-Tetrafluoro-4-mercaptobenzoic Acid
2,3,5,6-Tetrafluoro-4-mercaptobenzoic Acid is primarily used in the field of organic synthesis and material science. Its unique structure, featuring both thiol and carboxylic acid functional groups, makes it a valuable building block for creating complex molecules. It is often employed in the development of advanced polymers and coatings, where its fluorine atoms contribute to enhanced chemical resistance and durability. Additionally, this compound is utilized in the synthesis of pharmaceuticals and agrochemicals, where its reactive sites allow for precise modifications to achieve desired biological activities. In research, it serves as a key intermediate for studying thiol-based reactions and fluorine chemistry, aiding in the discovery of new materials and compounds with specialized properties.
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