(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-bromophenyl)propanoic acid
98%
- Product Code: 54792
CAS:
220497-79-0
| Molecular Weight: | 466.32 g./mol | Molecular Formula: | C₂₄H₂₀BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01311770 | |
| Melting Point: | 158.1°C | Boiling Point: | 657.1°C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the (9H-fluoren-9-yl)methoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine functionality. The bromophenyl moiety can be leveraged for further functionalization or as a handle in subsequent chemical modifications. Its application is crucial in the production of complex peptides and proteins, enabling precise control over the sequence and structure of the synthesized peptides. Additionally, the bromine atom on the phenyl ring can be exploited in cross-coupling reactions, making it valuable in the development of peptide-based therapeutics and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | €17.57 |
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| 1.000 | 10-20 days | €44.16 |
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| 5.000 | 10-20 days | €155.05 |
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| 10.000 | 10-20 days | €263.79 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-bromophenyl)propanoic acid
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the (9H-fluoren-9-yl)methoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine functionality. The bromophenyl moiety can be leveraged for further functionalization or as a handle in subsequent chemical modifications. Its application is crucial in the production of complex peptides and proteins, enabling precise control over the sequence and structure of the synthesized peptides. Additionally, the bromine atom on the phenyl ring can be exploited in cross-coupling reactions, making it valuable in the development of peptide-based therapeutics and bioactive molecules.
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