(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanamido)-4-methylpentanoic acid
95%
- Product Code: 232503
CAS:
88743-98-0
| Molecular Weight: | 466.57 g./mol | Molecular Formula: | C₂₇H₃₄N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01632054 | |
| Melting Point: | Boiling Point: | 695.5±45.0 °C(Predicted) | |
| Density: | 1.171±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in peptide synthesis as a protected amino acid derivative, enabling stepwise construction of complex peptides with stereochemical control. The Fmoc group allows for mild base-labile protection, facilitating solid-phase synthesis. Commonly employed in the preparation of branched peptides, peptide libraries, and bioconjugates for pharmaceutical and biochemical research. Its hydrophobic side chain supports solubility management in organic solvents during coupling steps. Also utilized in the development of peptide-based materials and drug discovery platforms.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,400.00 |
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| 1.000 | 10-20 days | ฿4,800.00 |
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| 5.000 | 10-20 days | ฿16,000.00 |
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| 25.000 | 10-20 days | ฿48,000.00 |
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(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanamido)-4-methylpentanoic acid
Used primarily in peptide synthesis as a protected amino acid derivative, enabling stepwise construction of complex peptides with stereochemical control. The Fmoc group allows for mild base-labile protection, facilitating solid-phase synthesis. Commonly employed in the preparation of branched peptides, peptide libraries, and bioconjugates for pharmaceutical and biochemical research. Its hydrophobic side chain supports solubility management in organic solvents during coupling steps. Also utilized in the development of peptide-based materials and drug discovery platforms.
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