2,4,6-Trifluorobenzaldehyde
>98.0%(GC)
- Product Code: 240048
CAS:
58551-83-0
| Molecular Weight: | 160.09 g./mol | Molecular Formula: | C₇H₃F₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00061197 | |
| Melting Point: | 60 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C, sealed |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atoms enhance metabolic stability and bioavailability. Employed in agrochemical manufacturing for creating herbicides and pesticides due to its ability to improve lipophilicity and target binding. Serves as a building block in liquid crystal materials for display technologies, contributing to mesogenic properties. Applied in research and development of specialty polymers and functional materials where fluorinated aromatics impart thermal and oxidative stability. Also utilized in the preparation of dyes and fluorescent probes, taking advantage of the electron-withdrawing fluorine groups to tune optical properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿340.00 |
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| 5.000 | 10-20 days | ฿1,580.00 |
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| 25.000 | 10-20 days | ฿7,390.00 |
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2,4,6-Trifluorobenzaldehyde
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atoms enhance metabolic stability and bioavailability. Employed in agrochemical manufacturing for creating herbicides and pesticides due to its ability to improve lipophilicity and target binding. Serves as a building block in liquid crystal materials for display technologies, contributing to mesogenic properties. Applied in research and development of specialty polymers and functional materials where fluorinated aromatics impart thermal and oxidative stability. Also utilized in the preparation of dyes and fluorescent probes, taking advantage of the electron-withdrawing fluorine groups to tune optical properties.
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