(2R,3S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxy-4-methylpentanoic acid
97%
- Product Code: 36485
CAS:
182959-73-5
| Molecular Weight: | 247.2881 g./mol | Molecular Formula: | C₁₁H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02682582 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of peptide-based drugs, where its chiral centers and protective groups are essential for controlling stereochemistry during synthesis. The tert-butoxycarbonyl (Boc) group provides stability and selectivity in reactions, making it valuable in the development of bioactive compounds. Additionally, it is employed in research for creating modified amino acids, which are crucial in studying enzyme mechanisms and designing inhibitors. Its structural features also make it suitable for use in solid-phase peptide synthesis, contributing to advancements in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,981.00 |
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(2R,3S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxy-4-methylpentanoic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of peptide-based drugs, where its chiral centers and protective groups are essential for controlling stereochemistry during synthesis. The tert-butoxycarbonyl (Boc) group provides stability and selectivity in reactions, making it valuable in the development of bioactive compounds. Additionally, it is employed in research for creating modified amino acids, which are crucial in studying enzyme mechanisms and designing inhibitors. Its structural features also make it suitable for use in solid-phase peptide synthesis, contributing to advancements in drug discovery and development.
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