tert-Butyl (S)-3-(aminooxy)pyrrolidine-1-carboxylate
98%
- Product Code: 233158
CAS:
952747-27-2
| Molecular Weight: | 202.25 g./mol | Molecular Formula: | C₉H₁₈N₂O₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 298.4±29.0 °C(Predicted) | |
| Density: | 1.12±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. The aminooxy group enables formation of oxime derivatives, making it valuable in bioconjugation, prodrug strategies, and the preparation of enzyme inhibitors. Its tert-butyloxycarbonyl (Boc) protection allows for selective deprotection and coupling in peptide-like synthesis, facilitating use in multi-step organic transformations. Commonly applied in medicinal chemistry for constructing nitrogen-containing heterocycles and in the design of protease inhibitors.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | $412.44 |
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| 250mg | 10-20 days | $1,308.80 |
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tert-Butyl (S)-3-(aminooxy)pyrrolidine-1-carboxylate
Used primarily as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. The aminooxy group enables formation of oxime derivatives, making it valuable in bioconjugation, prodrug strategies, and the preparation of enzyme inhibitors. Its tert-butyloxycarbonyl (Boc) protection allows for selective deprotection and coupling in peptide-like synthesis, facilitating use in multi-step organic transformations. Commonly applied in medicinal chemistry for constructing nitrogen-containing heterocycles and in the design of protease inhibitors.
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