1-Benzyl-3-(Boc-amino)pyrrolidine-3-carboxylic Acid
≥95%
- Product Code: 58232
CAS:
1027511-74-5
| Molecular Weight: | 320.38 g./mol | Molecular Formula: | C₁₇H₂₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09838930 | |
| Melting Point: | Boiling Point: | 474.1 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of various biologically active compounds, including potential drug candidates. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at other sites of the molecule, making it valuable in peptide synthesis and the construction of heterocyclic frameworks. Its application is significant in medicinal chemistry for designing molecules with specific therapeutic properties, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the development of prodrugs and other bioactive agents, contributing to advancements in drug discovery and optimization processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,280.00 |
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| 1.000 | 10-20 days | ฿12,600.00 |
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| 5.000 | 10-20 days | ฿53,460.00 |
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1-Benzyl-3-(Boc-amino)pyrrolidine-3-carboxylic Acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of various biologically active compounds, including potential drug candidates. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at other sites of the molecule, making it valuable in peptide synthesis and the construction of heterocyclic frameworks. Its application is significant in medicinal chemistry for designing molecules with specific therapeutic properties, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the development of prodrugs and other bioactive agents, contributing to advancements in drug discovery and optimization processes.
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