Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoate
95%
- Product Code: 58538
CAS:
86129-35-3
| Molecular Weight: | 297.32 g./mol | Molecular Formula: | C₁₅H₂₀FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24473468 | |
| Melting Point: | Boiling Point: | 406.9±40.0 °C(Predicted) | |
| Density: | 1.151±0.06 g/cm3(Predicted) | Storage Condition: | room temperature, inert atmosphere |
Product Description:
This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a fluorophenyl moiety, makes it valuable for constructing complex molecules with specific biological activities. It is often employed in medicinal chemistry research to create analogs of biologically active peptides, aiding in the study of enzyme inhibitors or receptor modulators. Additionally, its ester group allows for further chemical modifications, making it a versatile building block in organic synthesis. The fluorine atom enhances the compound's potential in drug design by influencing pharmacokinetic properties such as metabolic stability and binding affinity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,589.00 |
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| 0.250 | 10-20 days | ฿22,806.00 |
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Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoate
This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a fluorophenyl moiety, makes it valuable for constructing complex molecules with specific biological activities. It is often employed in medicinal chemistry research to create analogs of biologically active peptides, aiding in the study of enzyme inhibitors or receptor modulators. Additionally, its ester group allows for further chemical modifications, making it a versatile building block in organic synthesis. The fluorine atom enhances the compound's potential in drug design by influencing pharmacokinetic properties such as metabolic stability and binding affinity.
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