(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1-(tert-butoxycarbonyl)piperidin-4-yl)butanoic acid
97%
- Product Code: 236939
CAS:
313052-18-5
| Molecular Weight: | 508.61 g./mol | Molecular Formula: | C₂₉H₃₆N₂O₆ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide assembly. Its Fmoc group allows for mild base-labile protection of the alpha-amine, making it compatible with stepwise synthesis strategies that require repetitive deprotection. The tert-butoxycarbonyl (Boc) group on the piperidine ring provides orthogonal protection for side-chain functionalization, particularly useful in the synthesis of complex peptides containing modified amino acids. The structure supports the incorporation of conformationally constrained residues, aiding in the design of bioactive peptides with enhanced stability and receptor selectivity. It is especially valuable in the preparation of peptidomimetics and pharmaceutical intermediates where precise stereochemistry and side-chain protection are critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿2,350.00 |
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| 100mg | 10-20 days | ฿8,050.00 |
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| 250mg | 10-20 days | ฿19,930.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1-(tert-butoxycarbonyl)piperidin-4-yl)butanoic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide assembly. Its Fmoc group allows for mild base-labile protection of the alpha-amine, making it compatible with stepwise synthesis strategies that require repetitive deprotection. The tert-butoxycarbonyl (Boc) group on the piperidine ring provides orthogonal protection for side-chain functionalization, particularly useful in the synthesis of complex peptides containing modified amino acids. The structure supports the incorporation of conformationally constrained residues, aiding in the design of bioactive peptides with enhanced stability and receptor selectivity. It is especially valuable in the preparation of peptidomimetics and pharmaceutical intermediates where precise stereochemistry and side-chain protection are critical.
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