6-Amino-3-bromo-2-fluorobenzoic acid
97%
- Product Code: 120509
CAS:
1036756-03-2
| Molecular Weight: | 234.02 g./mol | Molecular Formula: | C₇H₅BrFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20482512 | |
| Melting Point: | Boiling Point: | 335.3±42.0 °C(Predicted) | |
| Density: | 1.877±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring amino, bromo, and fluoro substituents, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The bromo and fluoro groups are often leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, the amino group allows for further functionalization, enabling the synthesis of diverse derivatives. Its applications are particularly significant in medicinal chemistry, where it contributes to the creation of drug candidates targeting various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,836.00 |
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| 5.000 | 10-20 days | ฿6,201.00 |
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| 25.000 | 10-20 days | ฿23,148.00 |
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6-Amino-3-bromo-2-fluorobenzoic acid
This chemical is primarily utilized in organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring amino, bromo, and fluoro substituents, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The bromo and fluoro groups are often leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, the amino group allows for further functionalization, enabling the synthesis of diverse derivatives. Its applications are particularly significant in medicinal chemistry, where it contributes to the creation of drug candidates targeting various diseases.
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