Methyl 2-bromo-4-fluorobenzo[d]thiazole-6-carboxylate
≥95%
- Product Code: 116685
CAS:
924287-65-0
| Molecular Weight: | 290.11 g./mol | Molecular Formula: | C₉H₅BrFNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23705964 | |
| Melting Point: | Boiling Point: | 378.3±52.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of biologically active compounds, including potential drug candidates. The presence of both bromo and fluoro substituents makes it a useful precursor for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions. Additionally, its thiazole core is often explored in the design of compounds with antimicrobial, anti-inflammatory, or anticancer properties. In material science, it can be employed in the synthesis of organic electronic materials due to its aromatic structure and potential for conjugation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €114.68 |
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| 0.250 | 10-20 days | €183.30 |
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| 1.000 | 10-20 days | €385.84 |
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Methyl 2-bromo-4-fluorobenzo[d]thiazole-6-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of biologically active compounds, including potential drug candidates. The presence of both bromo and fluoro substituents makes it a useful precursor for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions. Additionally, its thiazole core is often explored in the design of compounds with antimicrobial, anti-inflammatory, or anticancer properties. In material science, it can be employed in the synthesis of organic electronic materials due to its aromatic structure and potential for conjugation.
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