(R)-3-(Benzyloxy)-2-(2-((tert-butoxycarbonyl)amino)-2-methylpropanamido)propanoic acid
95%
- Product Code: 96132
CAS:
159634-89-6
| Molecular Weight: | 380.44 g./mol | Molecular Formula: | C₁₉H₂₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12973663 | |
| Melting Point: | Boiling Point: | 592.0±50.0 °C(Predicted) | |
| Density: | 1.175±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a crucial intermediate. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable for safeguarding amino groups during the synthesis process. The benzyloxy group further enhances its utility by protecting hydroxyl functionalities, ensuring selective reactions can be carried out without unwanted side reactions.
In pharmaceutical research, it is employed to construct complex peptide chains, which are essential for developing therapeutic agents targeting various diseases. The compound’s stability and compatibility with standard peptide coupling reagents make it a preferred choice in solid-phase peptide synthesis (SPPS) and solution-phase methods. Additionally, its role in the synthesis of bioactive peptides and peptidomimetics underscores its importance in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,120.00 |
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| 0.250 | 10-20 days | ฿10,800.00 |
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| 1.000 | 10-20 days | ฿20,412.00 |
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(R)-3-(Benzyloxy)-2-(2-((tert-butoxycarbonyl)amino)-2-methylpropanamido)propanoic acid
This compound is primarily utilized in the field of peptide synthesis, where it serves as a crucial intermediate. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable for safeguarding amino groups during the synthesis process. The benzyloxy group further enhances its utility by protecting hydroxyl functionalities, ensuring selective reactions can be carried out without unwanted side reactions.
In pharmaceutical research, it is employed to construct complex peptide chains, which are essential for developing therapeutic agents targeting various diseases. The compound’s stability and compatibility with standard peptide coupling reagents make it a preferred choice in solid-phase peptide synthesis (SPPS) and solution-phase methods. Additionally, its role in the synthesis of bioactive peptides and peptidomimetics underscores its importance in drug discovery and development.
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