tert-Butyl 3-((3-bromopyridin-2-yl)oxy)azetidine-1-carboxylate
95%
- Product Code: 44304
CAS:
1227381-94-3
| Molecular Weight: | 329.1900 g./mol | Molecular Formula: | C₁₃H₁₇BrN₂O₃ |
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| EC Number: | MDL Number: | MFCD17012880 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the pharmaceutical industry for the preparation of biologically active compounds, particularly those targeting neurological disorders or as potential drug candidates. The presence of the bromopyridine moiety makes it a valuable building block for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating diverse chemical structures. Additionally, the azetidine ring and tert-butyloxycarbonyl (Boc) protecting group enhance its utility in peptide synthesis and medicinal chemistry, allowing for further functionalization and modification. Its application extends to agrochemical research, where it serves as a precursor for the synthesis of herbicides or pesticides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $114.67 |
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tert-Butyl 3-((3-bromopyridin-2-yl)oxy)azetidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the pharmaceutical industry for the preparation of biologically active compounds, particularly those targeting neurological disorders or as potential drug candidates. The presence of the bromopyridine moiety makes it a valuable building block for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating diverse chemical structures. Additionally, the azetidine ring and tert-butyloxycarbonyl (Boc) protecting group enhance its utility in peptide synthesis and medicinal chemistry, allowing for further functionalization and modification. Its application extends to agrochemical research, where it serves as a precursor for the synthesis of herbicides or pesticides.
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