(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1H-tetrazol-5-yl)butanoic acid
97%
- Product Code: 37428
CAS:
1464137-16-3
| Molecular Weight: | 393.40 g./mol | Molecular Formula: | C₂₀H₁₉N₅O₄ |
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| EC Number: | MDL Number: | MFCD26407301 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group serves as a temporary protecting group for the amino functionality, enabling selective deprotection during solid-phase peptide synthesis. The tetrazole moiety introduces unique properties, such as enhancing binding affinity or modifying the peptide's interaction with biological targets. It is often employed in the development of peptide-based drugs, where precise control over amino acid incorporation is critical. Additionally, its structure makes it valuable in the synthesis of peptidomimetics and bioactive compounds, particularly those targeting enzymes or receptors where tetrazole groups play a role in molecular recognition.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,304.00 |
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| 0.250 | 10-20 days | ฿4,608.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1H-tetrazol-5-yl)butanoic acid
This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group serves as a temporary protecting group for the amino functionality, enabling selective deprotection during solid-phase peptide synthesis. The tetrazole moiety introduces unique properties, such as enhancing binding affinity or modifying the peptide's interaction with biological targets. It is often employed in the development of peptide-based drugs, where precise control over amino acid incorporation is critical. Additionally, its structure makes it valuable in the synthesis of peptidomimetics and bioactive compounds, particularly those targeting enzymes or receptors where tetrazole groups play a role in molecular recognition.
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