4-Bromo-2-(2,2,2-trifluoroethoxy)pyridine
≥95%
- Product Code: 86143
CAS:
161952-62-1
| Molecular Weight: | 256.02 g./mol | Molecular Formula: | C₇H₅BrF₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13190652 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique combination of bromine and trifluoroethoxy groups makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse aromatic compounds. Meanwhile, the trifluoroethoxy group can impart desirable properties like increased metabolic stability or enhanced binding affinity in drug molecules. Additionally, it is employed in the research and development of new materials, particularly in the design of ligands for catalytic systems or in the modification of polymers to achieve specific electronic or chemical properties. Its role in these applications underscores its importance in advancing both medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,978.00 |
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| 0.250 | 10-20 days | ฿7,956.00 |
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4-Bromo-2-(2,2,2-trifluoroethoxy)pyridine
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique combination of bromine and trifluoroethoxy groups makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse aromatic compounds. Meanwhile, the trifluoroethoxy group can impart desirable properties like increased metabolic stability or enhanced binding affinity in drug molecules. Additionally, it is employed in the research and development of new materials, particularly in the design of ligands for catalytic systems or in the modification of polymers to achieve specific electronic or chemical properties. Its role in these applications underscores its importance in advancing both medicinal chemistry and material science.
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