(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)acetamido)-3-phenylpropanoic acid
95%
- Product Code: 232504
CAS:
117370-45-3
| Molecular Weight: | 444.47 g./mol | Molecular Formula: | C₂₆H₂₄N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00190882 | |
| Melting Point: | Boiling Point: | 739.5±60.0 °C(Predicted) | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used in peptide synthesis as a protected amino acid derivative, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection for the amino functionality, allowing selective deprotection under mild basic conditions while maintaining the integrity of other functional groups. The carboxylic acid group can be activated for amide bond formation with incoming amino acids, enabling stepwise assembly of peptides. Commonly employed in the preparation of complex peptides and proteins for research in biochemistry, drug development, and molecular biology. Its chiral center ensures stereochemical control during peptide chain elongation, making it valuable for synthesizing biologically active peptides with defined configurations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿10,470.00 |
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| 5.000 | 10-20 days | ฿34,730.00 |
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(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)acetamido)-3-phenylpropanoic acid
Used in peptide synthesis as a protected amino acid derivative, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection for the amino functionality, allowing selective deprotection under mild basic conditions while maintaining the integrity of other functional groups. The carboxylic acid group can be activated for amide bond formation with incoming amino acids, enabling stepwise assembly of peptides. Commonly employed in the preparation of complex peptides and proteins for research in biochemistry, drug development, and molecular biology. Its chiral center ensures stereochemical control during peptide chain elongation, making it valuable for synthesizing biologically active peptides with defined configurations.
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