Ethyl 2-bromo-4-fluorobenzoate
97%
- Product Code: 79260
CAS:
651341-68-3
| Molecular Weight: | 247.06 g./mol | Molecular Formula: | C₉H₈BrFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06204924 | |
| Melting Point: | Boiling Point: | 258.859°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromo and fluoro substituents, makes it valuable in the preparation of pharmaceuticals and agrochemicals. It serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly in the creation of compounds with potential therapeutic properties. Additionally, it is employed in research settings for the study of cross-coupling reactions, where the bromo group can facilitate palladium-catalyzed transformations. Its ester functionality also allows for further derivatization, making it a useful reagent in medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to light yellow to pale-brown Liquid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $13.80 |
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| 5.000 | 10-20 days | $48.00 |
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| 10.000 | 10-20 days | $59.41 |
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| 25.000 | 10-20 days | $183.62 |
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| 100.000 | 10-20 days | $558.06 |
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Ethyl 2-bromo-4-fluorobenzoate
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromo and fluoro substituents, makes it valuable in the preparation of pharmaceuticals and agrochemicals. It serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly in the creation of compounds with potential therapeutic properties. Additionally, it is employed in research settings for the study of cross-coupling reactions, where the bromo group can facilitate palladium-catalyzed transformations. Its ester functionality also allows for further derivatization, making it a useful reagent in medicinal chemistry and material science.
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