1-(2-Bromo-4-chlorophenyl)-2,2,2-trifluoroethanone
95%
- Product Code: 114332
CAS:
1033805-23-0
| Molecular Weight: | 287.46 g./mol | Molecular Formula: | C₈H₃BrClF₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27665766 | |
| Melting Point: | Boiling Point: | 277.1±40.0 °C(Predicted) | |
| Density: | 1.737±0.06 g/cm3(Predicted) | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromo and chloro substituents on the phenyl ring along with a trifluoroethanone group, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce functionalized aromatic rings into target compounds. Additionally, the trifluoroethanone moiety can serve as a precursor for the synthesis of trifluoromethyl-containing compounds, which are of significant interest in medicinal chemistry due to their enhanced metabolic stability and bioavailability. Its application is also seen in the development of herbicides and insecticides, where the halogenated aromatic core contributes to the biological activity of the final product.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿828.00 |
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| 1.000 | 10-20 days | ฿2,232.00 |
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| 5.000 | 10-20 days | ฿7,812.00 |
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1-(2-Bromo-4-chlorophenyl)-2,2,2-trifluoroethanone
This compound is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromo and chloro substituents on the phenyl ring along with a trifluoroethanone group, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce functionalized aromatic rings into target compounds. Additionally, the trifluoroethanone moiety can serve as a precursor for the synthesis of trifluoromethyl-containing compounds, which are of significant interest in medicinal chemistry due to their enhanced metabolic stability and bioavailability. Its application is also seen in the development of herbicides and insecticides, where the halogenated aromatic core contributes to the biological activity of the final product.
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