(S)-Ethyl 3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
95%
- Product Code: 57160
CAS:
67630-01-7
| Molecular Weight: | 308.37 g./mol | Molecular Formula: | C₁₆H₂₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18207036 | |
| Melting Point: | Boiling Point: | 471.1±40.0 °C(Predicted) | |
| Density: | 1.130±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, store away from light, inert atmosphere |
Product Description:
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring both an amino group and a protected amine, makes it valuable for constructing complex molecules with high precision. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, enhancing its utility in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft8,339.16 |
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| 0.250 | 10-20 days | Ft13,963.24 |
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| 1.000 | 10-20 days | Ft35,489.91 |
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(S)-Ethyl 3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring both an amino group and a protected amine, makes it valuable for constructing complex molecules with high precision. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, enhancing its utility in multi-step synthetic processes.
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