Ethyl 3-chloro-4-fluorobenzoate
≥98%
- Product Code: 78220
CAS:
137521-81-4
| Molecular Weight: | 202.61 g./mol | Molecular Formula: | C₉H₈ClFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06204341 | |
| Melting Point: | Boiling Point: | 255.4ºC | |
| Density: | 1.266g/cm3 | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as a building block for more complex molecules. It serves as an intermediate in the production of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require a fluorinated aromatic ring structure. Its chloro and fluoro substituents make it a valuable precursor for introducing these functional groups into target molecules, which can enhance biological activity or alter pharmacokinetic properties. Additionally, it is utilized in the synthesis of agrochemicals, where such functional groups are often critical for the efficacy of pesticides or herbicides. In research settings, it is employed in the study of chemical reactions involving halogenated aromatic compounds, aiding in the exploration of new synthetic pathways or reaction mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,026.00 |
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Ethyl 3-chloro-4-fluorobenzoate
This chemical is primarily used in organic synthesis as a building block for more complex molecules. It serves as an intermediate in the production of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require a fluorinated aromatic ring structure. Its chloro and fluoro substituents make it a valuable precursor for introducing these functional groups into target molecules, which can enhance biological activity or alter pharmacokinetic properties. Additionally, it is utilized in the synthesis of agrochemicals, where such functional groups are often critical for the efficacy of pesticides or herbicides. In research settings, it is employed in the study of chemical reactions involving halogenated aromatic compounds, aiding in the exploration of new synthetic pathways or reaction mechanisms.
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