ethyl 2,2-difluoro-2-(2-(trifluoromethyl)phenyl)acetate
98%
- Product Code: 74553
| Molecular Weight: | 268.18 g./mol | Molecular Formula: | C₁₁H₉F₅O₂ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
Ethyl 2,2-difluoro-2-(2-(trifluoromethyl)phenyl)acetate is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both difluoro and trifluoromethyl groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) where fluorine atoms enhance metabolic stability and bioavailability. Additionally, this compound is employed in agrochemical research for designing novel pesticides and herbicides, as the fluorine substituents often improve the efficacy and selectivity of these products. Its role in material science is also notable, where it contributes to the creation of advanced polymers and coatings with unique properties, such as increased resistance to environmental degradation.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colourless liquid |
| PURITY | 98-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | $18.48 |
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| 0.050 | 10-20 days | $48.37 |
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| 0.100 | 10-20 days | $171.07 |
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| 1.000 | 10-20 days | $601.29 |
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ethyl 2,2-difluoro-2-(2-(trifluoromethyl)phenyl)acetate
Ethyl 2,2-difluoro-2-(2-(trifluoromethyl)phenyl)acetate is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both difluoro and trifluoromethyl groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) where fluorine atoms enhance metabolic stability and bioavailability. Additionally, this compound is employed in agrochemical research for designing novel pesticides and herbicides, as the fluorine substituents often improve the efficacy and selectivity of these products. Its role in material science is also notable, where it contributes to the creation of advanced polymers and coatings with unique properties, such as increased resistance to environmental degradation.
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