Methyl 4-(trifluoromethyl)benzoate
99%
- Product Code: 205201
Alias:
Methyl 4-(trifluoromethyl)benzoate
Methyl para-trifluoromethylbenzoate
CAS:
2967-66-0
| Molecular Weight: | 204.15 g./mol | Molecular Formula: | C₉H₇F₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00042324 | |
| Melting Point: | 13-14 °C(lit.) | Boiling Point: | 94-95 °C21 mm Hg(lit.) |
| Density: | 1.268 g/mL at 25 °C(lit.) | Storage Condition: | Room temperature |
Product Description:
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for the preparation of bioactive molecules, including anti-inflammatory and central nervous system agents. Also utilized in the design of fluorinated analogs in structure-activity relationship (SAR) studies to improve potency and selectivity. 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 |
|---|---|---|---|
| 5g | 10-20 days | ฿270.00 |
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| 25g | 10-20 days | ฿410.00 |
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| 100g | 10-20 days | ฿1,450.00 |
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| 500g | 10-20 days | ฿6,800.00 |
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Methyl 4-(trifluoromethyl)benzoate
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for the preparation of bioactive molecules, including anti-inflammatory and central nervous system agents. Also utilized in the design of fluorinated analogs in structure-activity relationship (SAR) studies to improve potency and selectivity. 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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