(S)-N-Fmoc-2-(6'-octenyl)glycine
95%
- Product Code: 235121
CAS:
1058705-57-9
| Molecular Weight: | 378.46 g./mol | Molecular Formula: | C₂₄H₂₆O₄ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used in solid-phase peptide synthesis as a chiral building block for introducing a long-chain alkenyl-modified amino acid residue into peptide sequences. The Fmoc group allows for mild base-labile protection during stepwise synthesis, making it compatible with standard Fmoc-strategy protocols. The terminal alkene side chain serves as a handle for post-synthetic modifications, such as cross-metathesis or thiol-ene reactions, enabling site-specific conjugation to labels, polymers, or surfaces. Commonly applied in the development of bioconjugates, peptide-protein hybrids, and functional biomaterials where precise chemical modification is required. Its stereochemistry ensures correct folding and biological activity in chiral-sensitive peptides.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,520.00 |
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| 250mg | 10-20 days | ฿10,340.00 |
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| 1g | 10-20 days | ฿39,910.00 |
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(S)-N-Fmoc-2-(6'-octenyl)glycine
Used in solid-phase peptide synthesis as a chiral building block for introducing a long-chain alkenyl-modified amino acid residue into peptide sequences. The Fmoc group allows for mild base-labile protection during stepwise synthesis, making it compatible with standard Fmoc-strategy protocols. The terminal alkene side chain serves as a handle for post-synthetic modifications, such as cross-metathesis or thiol-ene reactions, enabling site-specific conjugation to labels, polymers, or surfaces. Commonly applied in the development of bioconjugates, peptide-protein hybrids, and functional biomaterials where precise chemical modification is required. Its stereochemistry ensures correct folding and biological activity in chiral-sensitive peptides.
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