Methyl 2,3,4-trifluorobenzoate
98%
- Product Code: 203133
CAS:
773873-68-0
| Molecular Weight: | 190.12 g./mol | Molecular Formula: | C₈H₅F₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06201866 | |
| Melting Point: | Boiling Point: | 214.3±40.0 °C(Predicted) | |
| Density: | 1.358±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive ester group and fluorine substitution pattern. The presence of three fluorine atoms enhances metabolic stability and bioavailability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, particularly in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in liquid crystal formulations for display technologies, where fluorinated aromatic cores improve thermal and electro-optical properties. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, making it a versatile building block in organic synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $28.71 |
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| 5.000 | 10-20 days | $137.37 |
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| 25.000 | 10-20 days | $658.77 |
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Methyl 2,3,4-trifluorobenzoate
Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive ester group and fluorine substitution pattern. The presence of three fluorine atoms enhances metabolic stability and bioavailability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, particularly in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in liquid crystal formulations for display technologies, where fluorinated aromatic cores improve thermal and electro-optical properties. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, making it a versatile building block in organic synthesis.
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