(S)-Methyl 2-(((benzyloxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoate
98%
- Product Code: 104370
CAS:
5068-29-1
| Molecular Weight: | 385.45 g./mol | Molecular Formula: | C₂₂H₂₇NO₅ |
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| EC Number: | MDL Number: | MFCD00237370 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of peptide-based drugs, where its structure aids in the protection of amino groups during complex reactions. Additionally, it is employed in the synthesis of biologically active molecules, contributing to the creation of compounds with potential therapeutic applications. Its tert-butoxy and benzyloxy groups provide stability and selectivity, making it valuable in multi-step synthetic processes. Researchers also leverage its chiral properties to develop enantiomerically pure substances, which are crucial in drug design to ensure efficacy and reduce side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $21.13 |
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| 5.000 | 10-20 days | $76.08 |
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| 25.000 | 10-20 days | $363.50 |
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(S)-Methyl 2-(((benzyloxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoate
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of peptide-based drugs, where its structure aids in the protection of amino groups during complex reactions. Additionally, it is employed in the synthesis of biologically active molecules, contributing to the creation of compounds with potential therapeutic applications. Its tert-butoxy and benzyloxy groups provide stability and selectivity, making it valuable in multi-step synthetic processes. Researchers also leverage its chiral properties to develop enantiomerically pure substances, which are crucial in drug design to ensure efficacy and reduce side effects.
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