tert-Butyl N-(6-fluoropyridin-2-yl)carbamate
≥95%
- Product Code: 82908
CAS:
891856-23-8
| Molecular Weight: | 212.22 g./mol | Molecular Formula: | C₁₀H₁₃FN₂O₂ |
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| EC Number: | MDL Number: | MFCD11976435 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring a fluoropyridine moiety and a tert-butyl carbamate group, makes it valuable in pharmaceutical research, particularly in the design of drug candidates. The fluorine atom enhances the molecule's reactivity and binding affinity, which is useful in creating biologically active molecules. It is often employed in the synthesis of agrochemicals and active pharmaceutical ingredients (APIs), where the fluoropyridine ring plays a critical role in improving the efficacy and stability of the final product. Additionally, its tert-butyl carbamate group serves as a protective group in peptide synthesis, ensuring selective reactions during complex molecular constructions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $278.90 |
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tert-Butyl N-(6-fluoropyridin-2-yl)carbamate
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring a fluoropyridine moiety and a tert-butyl carbamate group, makes it valuable in pharmaceutical research, particularly in the design of drug candidates. The fluorine atom enhances the molecule's reactivity and binding affinity, which is useful in creating biologically active molecules. It is often employed in the synthesis of agrochemicals and active pharmaceutical ingredients (APIs), where the fluoropyridine ring plays a critical role in improving the efficacy and stability of the final product. Additionally, its tert-butyl carbamate group serves as a protective group in peptide synthesis, ensuring selective reactions during complex molecular constructions.
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