N-Fmoc-2-amino-2-(2-propenyl)-4-Pentenoicacid,
97%
- Product Code: 217382
Alias:
2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-allyl-4-enic acid
CAS:
1311992-97-8
| Molecular Weight: | 377.44 g./mol | Molecular Formula: | C₂₃H₂₃NO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used in solid-phase peptide synthesis as a protected amino acid building block, particularly for incorporating unsaturated side chains into peptide structures. The Fmoc group allows for mild base-labile protection, compatible with stepwise elongation on resin. The allyl and pentenoyl moieties provide sites for post-assembly modifications, such as ring-closing metathesis, enabling the formation of cyclic peptides or constrained architectures. Commonly applied in the synthesis of bioactive peptide analogs and peptidomimetics where structural rigidity or specific side-chain functionality is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿3,060.00 |
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| 250mg | 10-20 days | ฿5,200.00 |
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| 1g | 10-20 days | ฿14,000.00 |
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| 5g | 10-20 days | ฿53,060.00 |
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N-Fmoc-2-amino-2-(2-propenyl)-4-Pentenoicacid,
Used in solid-phase peptide synthesis as a protected amino acid building block, particularly for incorporating unsaturated side chains into peptide structures. The Fmoc group allows for mild base-labile protection, compatible with stepwise elongation on resin. The allyl and pentenoyl moieties provide sites for post-assembly modifications, such as ring-closing metathesis, enabling the formation of cyclic peptides or constrained architectures. Commonly applied in the synthesis of bioactive peptide analogs and peptidomimetics where structural rigidity or specific side-chain functionality is required.
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| Stable in pH range | - |
| Solubility | - |
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| INCI | - |
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