Methyl 4-bromo-5-fluoro-2-methoxybenzoate
≥95%
- Product Code: 83957
CAS:
1084953-18-3
| Molecular Weight: | 263.06 g./mol | Molecular Formula: | C₉H₈BrFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23707518 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its functional groups, including the bromo and fluoro substituents, make it a valuable building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). The methoxy and ester groups further enhance its reactivity, enabling its use in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential for constructing drug-like molecules. Additionally, it serves as a precursor in the preparation of agrochemicals, where its halogenated aromatic ring contributes to the bioactivity of the final product. Its stability and reactivity also make it suitable for use in material science, particularly in the development of specialty polymers and coatings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft169,692.20 |
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| 0.250 | 10-20 days | Ft289,931.25 |
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Methyl 4-bromo-5-fluoro-2-methoxybenzoate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its functional groups, including the bromo and fluoro substituents, make it a valuable building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). The methoxy and ester groups further enhance its reactivity, enabling its use in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential for constructing drug-like molecules. Additionally, it serves as a precursor in the preparation of agrochemicals, where its halogenated aromatic ring contributes to the bioactivity of the final product. Its stability and reactivity also make it suitable for use in material science, particularly in the development of specialty polymers and coatings.
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