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 |
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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 |
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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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