2-Fluoro-4-(trifluoromethyl)benzoyl chloride
98%
- Product Code: 116140
CAS:
126917-10-0
| Molecular Weight: | 226.56 g./mol | Molecular Formula: | C₈H₃ClF₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00061155 | |
| Melting Point: | Boiling Point: | 188-189 °C (lit.) | |
| Density: | 1.5 g/mL at 25 °C (lit.) | Storage Condition: | room temperature |
Product Description:
Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the production of various pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to participate in Friedel-Crafts acylation reactions, forming complex aromatic ketones. These ketones are valuable building blocks in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the final compounds, making it a preferred choice in drug design. In agrochemicals, it contributes to the synthesis of herbicides and pesticides, where the fluorine atoms improve efficacy and environmental persistence. Its applications also extend to materials science, where it is used in the preparation of specialty polymers and coatings with unique properties such as chemical resistance and durability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,186.00 |
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| 5.000 | 10-20 days | ฿9,459.00 |
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2-Fluoro-4-(trifluoromethyl)benzoyl chloride
Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the production of various pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to participate in Friedel-Crafts acylation reactions, forming complex aromatic ketones. These ketones are valuable building blocks in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the final compounds, making it a preferred choice in drug design. In agrochemicals, it contributes to the synthesis of herbicides and pesticides, where the fluorine atoms improve efficacy and environmental persistence. Its applications also extend to materials science, where it is used in the preparation of specialty polymers and coatings with unique properties such as chemical resistance and durability.
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