(2S,4R)-4-((tert-Butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid
95%
- Product Code: 76144
CAS:
1279034-98-8
| Molecular Weight: | 230.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08704531 | |
| Melting Point: | Boiling Point: | 403.0±45.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a key building block for constructing complex peptide structures. Its tert-butoxycarbonyl (Boc) protecting group is particularly valuable in preventing unwanted reactions during the synthesis process, ensuring the desired peptide sequence is accurately formed. Additionally, it is employed in the development of pharmaceutical compounds, especially those targeting neurological and metabolic disorders, due to its ability to mimic natural amino acids and influence biological pathways. Its stereochemistry also plays a crucial role in enhancing the specificity and efficacy of the resulting peptides or drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £138.62 |
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| 0.250 | 10-20 days | £208.85 |
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| 1.000 | 10-20 days | £380.24 |
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(2S,4R)-4-((tert-Butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid
This compound is primarily utilized in the field of peptide synthesis, where it serves as a key building block for constructing complex peptide structures. Its tert-butoxycarbonyl (Boc) protecting group is particularly valuable in preventing unwanted reactions during the synthesis process, ensuring the desired peptide sequence is accurately formed. Additionally, it is employed in the development of pharmaceutical compounds, especially those targeting neurological and metabolic disorders, due to its ability to mimic natural amino acids and influence biological pathways. Its stereochemistry also plays a crucial role in enhancing the specificity and efficacy of the resulting peptides or drugs.
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