Methyl 3-bromo-5-fluoro-4-nitrobenzoate
≥95%
- Product Code: 66304
CAS:
1123171-93-6
| Molecular Weight: | 278.03 g./mol | Molecular Formula: | C₈H₅BrFNO₄ |
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| EC Number: | MDL Number: | MFCD14635859 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
Methyl 3-bromo-5-fluoro-4-nitrobenzoate is primarily used in organic synthesis as an intermediate compound. Its structure, featuring bromo, fluoro, and nitro groups, makes it a valuable building block for constructing more complex molecules, particularly in pharmaceutical and agrochemical research. The compound is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to participate in various chemical reactions, such as nucleophilic substitution and coupling reactions. Additionally, its nitro group can be reduced to form amines, which are crucial in the synthesis of many drugs. In agrochemicals, it serves as a precursor for creating herbicides, fungicides, and insecticides, leveraging its halogenated aromatic properties to enhance biological activity. Its versatility and reactivity make it a key component in the design and production of specialized chemical products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,707.00 |
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| 0.250 | 10-20 days | ฿8,199.00 |
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| 1.000 | 10-20 days | ฿20,529.00 |
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| 5.000 | 10-20 days | ฿57,681.00 |
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Methyl 3-bromo-5-fluoro-4-nitrobenzoate
Methyl 3-bromo-5-fluoro-4-nitrobenzoate is primarily used in organic synthesis as an intermediate compound. Its structure, featuring bromo, fluoro, and nitro groups, makes it a valuable building block for constructing more complex molecules, particularly in pharmaceutical and agrochemical research. The compound is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to participate in various chemical reactions, such as nucleophilic substitution and coupling reactions. Additionally, its nitro group can be reduced to form amines, which are crucial in the synthesis of many drugs. In agrochemicals, it serves as a precursor for creating herbicides, fungicides, and insecticides, leveraging its halogenated aromatic properties to enhance biological activity. Its versatility and reactivity make it a key component in the design and production of specialized chemical products.
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