Diethyl (4-fluorobenzoyl)malonate
95%
- Product Code: 82893
CAS:
174403-79-3
| Molecular Weight: | 282.26 g./mol | Molecular Formula: | C₁₄H₁₅FO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29081542 | |
| Melting Point: | Boiling Point: | 341.4±27.0 °C(Predicted) | |
| Density: | 1.218±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
Diethyl (4-fluorobenzoyl)malonate is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It plays a key role in the construction of complex molecules due to its reactive malonate ester group, which can undergo various transformations such as alkylation, condensation, and cyclization. This compound is often utilized in the synthesis of fluorinated aromatic compounds, which are valuable in drug development for their enhanced biological activity and stability. Additionally, it serves as a building block for the preparation of heterocyclic compounds, which are widely used in medicinal chemistry. Its application extends to the development of active ingredients in pesticides and herbicides, leveraging the fluorine atom's ability to improve efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿567.00 |
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| 5.000 | 10-20 days | ฿1,971.00 |
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| 25.000 | 10-20 days | ฿6,894.00 |
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Diethyl (4-fluorobenzoyl)malonate
Diethyl (4-fluorobenzoyl)malonate is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It plays a key role in the construction of complex molecules due to its reactive malonate ester group, which can undergo various transformations such as alkylation, condensation, and cyclization. This compound is often utilized in the synthesis of fluorinated aromatic compounds, which are valuable in drug development for their enhanced biological activity and stability. Additionally, it serves as a building block for the preparation of heterocyclic compounds, which are widely used in medicinal chemistry. Its application extends to the development of active ingredients in pesticides and herbicides, leveraging the fluorine atom's ability to improve efficacy and selectivity.
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