(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenylpyrrolidine-2-carboxylic acid
≥95%
- Product Code: 51146
CAS:
96314-29-3
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321010 | |
| Melting Point: | Boiling Point: | 441.5°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its structure makes it a valuable intermediate for constructing complex molecules, especially in the production of protease inhibitors and other bioactive compounds. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines during synthetic processes, ensuring selective reactions and preventing unwanted side reactions. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which is crucial for drug efficacy and safety. It is also employed in research for studying enzyme interactions and designing new therapeutic agents targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $148.78 |
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| 0.250 | 10-20 days | $251.49 |
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| 1.000 | 10-20 days | $606.54 |
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(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenylpyrrolidine-2-carboxylic acid
This chemical is primarily used in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its structure makes it a valuable intermediate for constructing complex molecules, especially in the production of protease inhibitors and other bioactive compounds. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines during synthetic processes, ensuring selective reactions and preventing unwanted side reactions. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which is crucial for drug efficacy and safety. It is also employed in research for studying enzyme interactions and designing new therapeutic agents targeting specific biological pathways.
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