(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-cyanobutanoicacid
97%
- Product Code: 237805
CAS:
913253-24-4
| Molecular Weight: | 350.37 g./mol | Molecular Formula: | C₂₀H₁₈N₂O₄ |
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| EC Number: | MDL Number: | MFCD02092980 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions in the production of complex peptides and proteins. The Fmoc group provides base-labile protection for the amine functionality, allowing stepwise assembly under mild conditions. The nitrile side chain can be further modified or used to influence peptide conformation and stability. Commonly applied in solid-phase peptide synthesis (SPPS), particularly for generating bioactive peptides with specific structural features. Its chiral purity ensures correct stereochemistry in the final product, which is critical for biological activity in pharmaceutical research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | $118.92 |
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| 100mg | 10-20 days | $276.56 |
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| 250mg | 10-20 days | $527.97 |
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| 1g | 10-20 days | $1,397.14 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-cyanobutanoicacid
Used primarily in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions in the production of complex peptides and proteins. The Fmoc group provides base-labile protection for the amine functionality, allowing stepwise assembly under mild conditions. The nitrile side chain can be further modified or used to influence peptide conformation and stability. Commonly applied in solid-phase peptide synthesis (SPPS), particularly for generating bioactive peptides with specific structural features. Its chiral purity ensures correct stereochemistry in the final product, which is critical for biological activity in pharmaceutical research.
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