(S)-2-((((Benzyloxy)carbonyl)amino)methyl)-3-methylbutanoic acid
97%
- Product Code: 38057
CAS:
631899-14-4
| Molecular Weight: | 265.3050 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28005478 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable in organic chemistry for protecting amine groups during complex reactions. It is often employed in the production of bioactive molecules and drug candidates, particularly in the development of protease inhibitors and other therapeutic agents. Additionally, it serves as a building block in medicinal chemistry for creating chiral compounds, ensuring high enantiomeric purity in the final products. Its application extends to research in biochemistry and pharmacology, where it aids in studying enzyme mechanisms and designing targeted therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,883.00 |
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(S)-2-((((Benzyloxy)carbonyl)amino)methyl)-3-methylbutanoic acid
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable in organic chemistry for protecting amine groups during complex reactions. It is often employed in the production of bioactive molecules and drug candidates, particularly in the development of protease inhibitors and other therapeutic agents. Additionally, it serves as a building block in medicinal chemistry for creating chiral compounds, ensuring high enantiomeric purity in the final products. Its application extends to research in biochemistry and pharmacology, where it aids in studying enzyme mechanisms and designing targeted therapies.
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