1-(6-Bromopyridin-3-yl)-2,2,2-trifluoroethanone hydrate
≥95%
- Product Code: 114484
CAS:
1956366-86-1
| Molecular Weight: | 272.02 g./mol | Molecular Formula: | C₇H₅BrF₃NO₂ |
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| EC Number: | MDL Number: | MFCD28016685 | |
| 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, particularly as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety and a trifluoroethanone group, makes it valuable for constructing complex molecules, especially those requiring halogenated aromatic systems. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine rings into target molecules. Additionally, its trifluoroethanone group can serve as a precursor for further transformations, enabling the synthesis of biologically active compounds. Its application extends to materials science, where it contributes to the creation of specialized polymers and ligands for catalytic systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $117.08 |
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| 0.250 | 10-20 days | $233.70 |
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1-(6-Bromopyridin-3-yl)-2,2,2-trifluoroethanone hydrate
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety and a trifluoroethanone group, makes it valuable for constructing complex molecules, especially those requiring halogenated aromatic systems. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine rings into target molecules. Additionally, its trifluoroethanone group can serve as a precursor for further transformations, enabling the synthesis of biologically active compounds. Its application extends to materials science, where it contributes to the creation of specialized polymers and ligands for catalytic systems.
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