tert-Butyl 3-((6-bromopyridin-3-yl)oxy)azetidine-1-carboxylate
95%
- Product Code: 44162
CAS:
1146089-80-6
| Molecular Weight: | 329.1897 g./mol | Molecular Formula: | C₁₃H₁₇BrN₂O₃ |
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| EC Number: | MDL Number: | MFCD22987896 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a bromopyridine moiety and an azetidine ring, makes it valuable for constructing molecules with potential therapeutic applications, particularly in the fields of oncology and neurology. It is often employed in the preparation of small-molecule inhibitors targeting specific enzymes or receptors. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its versatility in organic synthesis. Researchers also explore its use in the development of agrochemicals and other specialty chemicals due to its unique reactivity and functional group compatibility.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €215.12 |
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tert-Butyl 3-((6-bromopyridin-3-yl)oxy)azetidine-1-carboxylate
This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a bromopyridine moiety and an azetidine ring, makes it valuable for constructing molecules with potential therapeutic applications, particularly in the fields of oncology and neurology. It is often employed in the preparation of small-molecule inhibitors targeting specific enzymes or receptors. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its versatility in organic synthesis. Researchers also explore its use in the development of agrochemicals and other specialty chemicals due to its unique reactivity and functional group compatibility.
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