(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid
97%
- Product Code: 235011
CAS:
116611-64-4
| Molecular Weight: | 377.39 g./mol | Molecular Formula: | C₂₁H₁₉N₃O₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 706.7±60.0°C | |
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for histidine residues with defined stereochemistry. Its Fmoc group allows for mild base-labile protection, enabling stepwise assembly of peptides in solid-phase synthesis. The imidazole side chain remains stable during coupling and deprotection steps, making it ideal for preparing biologically active peptides that require histidine for function or structure. It is especially valuable in pharmaceutical research, including the development of peptide-based drugs and diagnostic agents.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿174.00 |
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| 1g | 10-20 days | ฿360.00 |
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| 5g | 10-20 days | ฿1,480.00 |
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| 25g | 10-20 days | ฿6,250.00 |
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| 100g | 10-20 days | ฿20,500.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for histidine residues with defined stereochemistry. Its Fmoc group allows for mild base-labile protection, enabling stepwise assembly of peptides in solid-phase synthesis. The imidazole side chain remains stable during coupling and deprotection steps, making it ideal for preparing biologically active peptides that require histidine for function or structure. It is especially valuable in pharmaceutical research, including the development of peptide-based drugs and diagnostic agents.
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