Methyl 4-bromo-2,3-difluorobenzoate
98%
- Product Code: 47329
CAS:
1807244-07-0
Molecular Weight: | 251.0249 g./mol | Molecular Formula: | C₈H₅BrF₂O₂ |
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EC Number: | MDL Number: | MFCD27578309 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Methyl 4-bromo-2,3-difluorobenzoate is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block for creating more complex molecules. In pharmaceutical research, it is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the presence of halogen atoms can enhance biological activity or improve drug stability. Additionally, it is utilized in the production of agrochemicals, such as herbicides and pesticides, where the difluoro and bromo groups contribute to the efficacy of the final product. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also significant, enabling the construction of diverse aromatic compounds with specific functional properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,088.00 |
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Methyl 4-bromo-2,3-difluorobenzoate
Methyl 4-bromo-2,3-difluorobenzoate is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block for creating more complex molecules. In pharmaceutical research, it is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the presence of halogen atoms can enhance biological activity or improve drug stability. Additionally, it is utilized in the production of agrochemicals, such as herbicides and pesticides, where the difluoro and bromo groups contribute to the efficacy of the final product. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also significant, enabling the construction of diverse aromatic compounds with specific functional properties.
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