ethyl 2-(3-bromophenyl)-2,2-difluoroacetate
90%
- Product Code: 74619
CAS:
885068-75-7
| Molecular Weight: | 279.08 g./mol | Molecular Formula: | C₁₀H₉BrF₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily used in the synthesis of more complex organic compounds, particularly in pharmaceutical research. It serves as a key intermediate in the development of various active pharmaceutical ingredients (APIs). The presence of the difluoroacetate group makes it valuable for introducing fluorine atoms into target molecules, which can enhance their biological activity, metabolic stability, and bioavailability. Additionally, the bromophenyl moiety provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical structures. Its applications are largely focused on medicinal chemistry, where it contributes to the discovery and optimization of drug candidates.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,770.00 |
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| 1.000 | 10-20 days | ฿15,520.00 |
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| 5.000 | 10-20 days | ฿39,520.00 |
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ethyl 2-(3-bromophenyl)-2,2-difluoroacetate
This chemical is primarily used in the synthesis of more complex organic compounds, particularly in pharmaceutical research. It serves as a key intermediate in the development of various active pharmaceutical ingredients (APIs). The presence of the difluoroacetate group makes it valuable for introducing fluorine atoms into target molecules, which can enhance their biological activity, metabolic stability, and bioavailability. Additionally, the bromophenyl moiety provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical structures. Its applications are largely focused on medicinal chemistry, where it contributes to the discovery and optimization of drug candidates.
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