Fmoc-L-2-amino-4-bromo-4-pentenoic acid
≥95%
- Product Code: 105063
CAS:
220497-60-9
| Molecular Weight: | 413.27 g./mol | Molecular Formula: | C₂₀H₁₈BrNO₄ |
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| EC Number: | MDL Number: | MFCD01311750 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild basic conditions, making it suitable for constructing complex peptides. The bromoalkene functional group in the molecule provides a reactive site for further modifications, such as cross-coupling reactions, enabling the introduction of diverse chemical functionalities into peptide chains. This makes it valuable in the development of peptide-based drugs, biomaterials, and research tools. Additionally, its unique structure can be employed in the synthesis of peptidomimetics and other bioactive molecules, where the bromoalkene moiety can serve as a handle for post-synthetic modifications or as a key structural element in the final product.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,828.00 |
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Fmoc-L-2-amino-4-bromo-4-pentenoic acid
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild basic conditions, making it suitable for constructing complex peptides. The bromoalkene functional group in the molecule provides a reactive site for further modifications, such as cross-coupling reactions, enabling the introduction of diverse chemical functionalities into peptide chains. This makes it valuable in the development of peptide-based drugs, biomaterials, and research tools. Additionally, its unique structure can be employed in the synthesis of peptidomimetics and other bioactive molecules, where the bromoalkene moiety can serve as a handle for post-synthetic modifications or as a key structural element in the final product.
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