(S)-1-Benzyl 4-methyl 2-((tert-butoxycarbonyl)amino)succinate
95%
- Product Code: 37984
CAS:
158201-15-1
| Molecular Weight: | 337.37 g./mol | Molecular Formula: | C₁₇H₂₃NO₆ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of peptides and complex organic molecules, serving as a key intermediate in pharmaceutical research. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide coupling reactions, where selective protection and deprotection of amino groups are required. The benzyl ester group enhances solubility in organic solvents, facilitating its use in various chemical transformations. Additionally, it is employed in the development of chiral compounds, leveraging its stereocenter to induce enantioselectivity in asymmetric synthesis. Its applications extend to the production of bioactive molecules, including potential drug candidates targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $59.43 |
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(S)-1-Benzyl 4-methyl 2-((tert-butoxycarbonyl)amino)succinate
This compound is primarily utilized in the synthesis of peptides and complex organic molecules, serving as a key intermediate in pharmaceutical research. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide coupling reactions, where selective protection and deprotection of amino groups are required. The benzyl ester group enhances solubility in organic solvents, facilitating its use in various chemical transformations. Additionally, it is employed in the development of chiral compounds, leveraging its stereocenter to induce enantioselectivity in asymmetric synthesis. Its applications extend to the production of bioactive molecules, including potential drug candidates targeting specific biological pathways.
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