(R)-3-((((9H-Ffluoren-9-yl)methoxy)carbonyl)amino)-4-(4-bromophenyl)butanoic acid
98%
- Product Code: 81908
CAS:
331763-76-9
| Molecular Weight: | 480.350 g./mol | Molecular Formula: | C₂₅H₂₂BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01860918 | |
| Melting Point: | Boiling Point: | 673.0±55.0 °C at 760 mmHg | |
| Density: | 1.4±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in peptide synthesis as a building block for the introduction of specific amino acid residues. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the Fmoc (fluorenylmethoxycarbonyl) protecting group, which can be selectively removed under mild basic conditions. The bromophenyl moiety allows for further functionalization or conjugation, making it useful in the development of peptide-based drugs, bioconjugates, or probes for biochemical studies. Its application extends to research in medicinal chemistry, where it aids in the design and synthesis of peptides with targeted biological activity. Additionally, it can be employed in the study of enzyme-substrate interactions or as a precursor for more complex organic molecules in pharmaceutical development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,016.00 |
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| 0.250 | 10-20 days | ฿3,024.00 |
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| 1.000 | 10-20 days | ฿7,461.00 |
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(R)-3-((((9H-Ffluoren-9-yl)methoxy)carbonyl)amino)-4-(4-bromophenyl)butanoic acid
This compound is primarily utilized in peptide synthesis as a building block for the introduction of specific amino acid residues. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the Fmoc (fluorenylmethoxycarbonyl) protecting group, which can be selectively removed under mild basic conditions. The bromophenyl moiety allows for further functionalization or conjugation, making it useful in the development of peptide-based drugs, bioconjugates, or probes for biochemical studies. Its application extends to research in medicinal chemistry, where it aids in the design and synthesis of peptides with targeted biological activity. Additionally, it can be employed in the study of enzyme-substrate interactions or as a precursor for more complex organic molecules in pharmaceutical development.
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