(R)-Methyl 2-amino-4-((tert-butoxycarbonyl)amino)butanoate hydrochloride
95%
- Product Code: 123671
CAS:
1052649-77-0
| Molecular Weight: | 268.74 g./mol | Molecular Formula: | C₁₀H₂₁ClN₂O₄ |
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| EC Number: | MDL Number: | MFCD08275859 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a protected amino group and an ester functionality, makes it a valuable building block in organic synthesis. It is often employed in the preparation of chiral molecules, where the (R)-configuration is crucial for biological activity. Additionally, it serves as a precursor in the production of specialized amino acid derivatives used in drug discovery and medicinal chemistry. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,818.00 |
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| 1.000 | 10-20 days | ฿4,905.00 |
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| 5.000 | 10-20 days | ฿17,145.00 |
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(R)-Methyl 2-amino-4-((tert-butoxycarbonyl)amino)butanoate hydrochloride
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a protected amino group and an ester functionality, makes it a valuable building block in organic synthesis. It is often employed in the preparation of chiral molecules, where the (R)-configuration is crucial for biological activity. Additionally, it serves as a precursor in the production of specialized amino acid derivatives used in drug discovery and medicinal chemistry. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes.
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