3-Fluoro-4-(trifluoromethyl)benzoyl chloride
95%
- Product Code: 188335
CAS:
216144-68-2
| Molecular Weight: | 226.56 g./mol | Molecular Formula: | C₈H₃ClF₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00236284 | |
| Melting Point: | 152 °C | Boiling Point: | |
| Density: | 1.486 g/mL at 25 °C (lit.) | Storage Condition: | Room temperature |
Product Description:
Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for the introduction of fluorinated aromatic moieties, which can enhance the bioavailability and metabolic stability of active compounds. Commonly employed in the production of herbicides and fungicides due to the electron-withdrawing properties of the trifluoromethyl and fluoro groups, which improve binding to biological targets. Also utilized in the preparation of specialty polymers and liquid crystals where fluorination contributes to thermal and chemical resistance. Reacts readily with nucleophiles such as amines and alcohols, making it valuable in constructing complex molecules through amide or ester formation.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿3,050.00 |
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| 5g | 10-20 days | ฿6,130.00 |
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| 25g | 10-20 days | ฿29,830.00 |
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| 250mg | 10-20 days | ฿1,270.00 |
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3-Fluoro-4-(trifluoromethyl)benzoyl chloride
Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for the introduction of fluorinated aromatic moieties, which can enhance the bioavailability and metabolic stability of active compounds. Commonly employed in the production of herbicides and fungicides due to the electron-withdrawing properties of the trifluoromethyl and fluoro groups, which improve binding to biological targets. Also utilized in the preparation of specialty polymers and liquid crystals where fluorination contributes to thermal and chemical resistance. Reacts readily with nucleophiles such as amines and alcohols, making it valuable in constructing complex molecules through amide or ester formation.
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