(S)-Ethyl 3-((tert-butoxycarbonyl)amino)butanoate
97%
- Product Code: 38384
CAS:
166194-56-5
| Molecular Weight: | 231.2887 g./mol | Molecular Formula: | C₁₁H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29077191 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a key role in the production of chiral molecules, where its stereochemistry is crucial for the desired biological activity of the final product. It is often employed in the preparation of peptides and peptidomimetics, contributing to the development of drugs targeting various diseases. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, ensuring the integrity of the amino functionality during chemical transformations. This compound is also utilized in research settings for studying enzyme mechanisms and designing bioactive molecules with specific properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $144.98 |
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(S)-Ethyl 3-((tert-butoxycarbonyl)amino)butanoate
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a key role in the production of chiral molecules, where its stereochemistry is crucial for the desired biological activity of the final product. It is often employed in the preparation of peptides and peptidomimetics, contributing to the development of drugs targeting various diseases. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, ensuring the integrity of the amino functionality during chemical transformations. This compound is also utilized in research settings for studying enzyme mechanisms and designing bioactive molecules with specific properties.
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