Methyl 6-bromo-2-fluoro-3-(trifluoromethyl)benzoate

97%

  • Product Code: 49856
  CAS:    1352718-55-8
Molecular Weight: 301.0324 g./mol Molecular Formula: C₉H₅BrF₄O₂
EC Number: MDL Number: MFCD28134146
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of more complex molecules. Its structure, featuring bromo, fluoro, and trifluoromethyl groups, makes it a valuable building block for creating compounds with specific biological activities. In pharmaceuticals, it can be utilized in the development of active ingredients for drugs targeting various diseases, particularly those requiring molecules with fluorine substituents for enhanced stability and bioavailability. In agrochemicals, it serves as a precursor in the production of pesticides or herbicides, where the trifluoromethyl group often contributes to increased efficacy and selectivity. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical entities for research and development purposes.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿4,374.00
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Methyl 6-bromo-2-fluoro-3-(trifluoromethyl)benzoate
This compound is primarily used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of more complex molecules. Its structure, featuring bromo, fluoro, and trifluoromethyl groups, makes it a valuable building block for creating compounds with specific biological activities. In pharmaceuticals, it can be utilized in the development of active ingredients for drugs targeting various diseases, particularly those requiring molecules with fluorine substituents for enhanced stability and bioavailability. In agrochemicals, it serves as a precursor in the production of pesticides or herbicides, where the trifluoromethyl group often contributes to increased efficacy and selectivity. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical entities for research and development purposes.
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