(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-vinylphenyl)propanoic acid
95%
- Product Code: 236638
CAS:
1270295-57-2
| Molecular Weight: | 413.47 g./mol | Molecular Formula: | C₂₆H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09951904 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, light-proof |
Product Description:
Used in peptide synthesis as a chiral building block for introducing phenylalanine derivatives with a vinyl-functionalized side chain. The vinyl group allows for post-synthetic modifications via cross-coupling reactions or polymerization, making it valuable in the development of functionalized biomaterials, bioconjugates, or stimuli-responsive peptides. The Fmoc protection enables compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly of custom sequences under mild basic conditions. Its stereochemistry ensures enantioselective incorporation, which is critical for maintaining biological activity in synthetic peptides.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿8,400.00 |
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| 250mg | 10-20 days | ฿33,580.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-vinylphenyl)propanoic acid
Used in peptide synthesis as a chiral building block for introducing phenylalanine derivatives with a vinyl-functionalized side chain. The vinyl group allows for post-synthetic modifications via cross-coupling reactions or polymerization, making it valuable in the development of functionalized biomaterials, bioconjugates, or stimuli-responsive peptides. The Fmoc protection enables compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly of custom sequences under mild basic conditions. Its stereochemistry ensures enantioselective incorporation, which is critical for maintaining biological activity in synthetic peptides.
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