(S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoate
95%
- Product Code: 233341
CAS:
160450-10-2
| Molecular Weight: | 391.42 g./mol | Molecular Formula: | C₂₂H₂₁N₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27578253 | |
| Melting Point: | 113-115 °C | Boiling Point: | 671.6±55.0 °C(Predicted) |
| Density: | 1.303±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in peptide synthesis as a protected histidine derivative, enabling selective and efficient coupling in solid-phase peptide synthesis. The Fmoc group allows for mild base deprotection, making it compatible with sensitive amino acid sequences. Its stereochemistry ensures chiral integrity during peptide chain assembly, particularly in the production of therapeutic peptides and biochemical research tools. Commonly employed in automated synthesizers for generating antigens, enzyme substrates, and receptor ligands.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,730.00 |
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| 250mg | 10-20 days | ฿4,630.00 |
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| 1g | 10-20 days | ฿12,470.00 |
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(S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoate
Widely used in peptide synthesis as a protected histidine derivative, enabling selective and efficient coupling in solid-phase peptide synthesis. The Fmoc group allows for mild base deprotection, making it compatible with sensitive amino acid sequences. Its stereochemistry ensures chiral integrity during peptide chain assembly, particularly in the production of therapeutic peptides and biochemical research tools. Commonly employed in automated synthesizers for generating antigens, enzyme substrates, and receptor ligands.
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