(S)-tert-Butyl (2-oxopyrrolidin-3-yl)carbamate
97%
- Product Code: 235076
CAS:
92235-34-2
| Molecular Weight: | 200.24 g./mol | Molecular Formula: | C₉H₁₆N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs like piracetam and related racetam family compounds. Its protected amine and ketone functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis due to the stereochemistry at the 3-position of the pyrrolidone ring, enabling the development of enantiomerically pure active pharmaceutical ingredients. Also utilized in the preparation of enzyme inhibitors and cognitive enhancers.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | white solid |
| Purity (%) | 96.5-100% |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿710.00 |
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| 100mg | 10-20 days | ฿1,350.00 |
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| 250mg | 10-20 days | ฿2,260.00 |
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| 1g | 10-20 days | ฿7,650.00 |
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| bulk | 10-20 days | ฿0.00 |
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| 5g | 10-20 days | ฿38,250.00 |
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(S)-tert-Butyl (2-oxopyrrolidin-3-yl)carbamate
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs like piracetam and related racetam family compounds. Its protected amine and ketone functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis due to the stereochemistry at the 3-position of the pyrrolidone ring, enabling the development of enantiomerically pure active pharmaceutical ingredients. Also utilized in the preparation of enzyme inhibitors and cognitive enhancers.
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| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
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