(S)-2-(((Benzyloxy)carbonyl)amino)-3-(2-fluorophenyl)propanoic acid
≥95%
- Product Code: 51109
CAS:
127862-88-8
| Molecular Weight: | 317.31 g./mol | Molecular Formula: | C₁₇H₁₆FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00797567 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring a fluorophenyl group, makes it valuable for developing compounds with enhanced binding affinity and selectivity towards specific receptors or enzymes. Researchers often employ it in the design and optimization of peptide-based drugs, where its chiral center ensures the desired stereochemistry in the final product. Additionally, its benzyloxycarbonyl (Cbz) protecting group allows for controlled deprotection during multi-step synthetic processes, making it a versatile building block in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,178.00 |
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| 0.250 | 10-20 days | ฿3,267.00 |
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| 1.000 | 10-20 days | ฿8,226.00 |
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(S)-2-(((Benzyloxy)carbonyl)amino)-3-(2-fluorophenyl)propanoic acid
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring a fluorophenyl group, makes it valuable for developing compounds with enhanced binding affinity and selectivity towards specific receptors or enzymes. Researchers often employ it in the design and optimization of peptide-based drugs, where its chiral center ensures the desired stereochemistry in the final product. Additionally, its benzyloxycarbonyl (Cbz) protecting group allows for controlled deprotection during multi-step synthetic processes, making it a versatile building block in organic synthesis.
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