(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(methylamino)-5-oxopentanoic acid
95%
- Product Code: 232836
CAS:
1446478-17-6
| Molecular Weight: | 382.41 g./mol | Molecular Formula: | C₂₁H₂₂N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31706201 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in peptide synthesis as a protected amino acid building block. The Fmoc group enables solid-phase peptide synthesis by providing temporary N-terminal protection that is easily removed under mild basic conditions, allowing stepwise assembly of peptide chains. The methylamino group can participate in coupling reactions to extend the peptide backbone or introduce specific side chains. Its stereochemistry ensures chiral purity in the synthesized peptides, making it valuable in pharmaceutical research and development of bioactive peptides. Commonly employed in the production of peptide-based drugs, diagnostics, and biochemical probes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿9,600.00 |
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| 250mg | 10-20 days | ฿16,000.00 |
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| 500mg | 10-20 days | ฿26,660.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(methylamino)-5-oxopentanoic acid
Used primarily in peptide synthesis as a protected amino acid building block. The Fmoc group enables solid-phase peptide synthesis by providing temporary N-terminal protection that is easily removed under mild basic conditions, allowing stepwise assembly of peptide chains. The methylamino group can participate in coupling reactions to extend the peptide backbone or introduce specific side chains. Its stereochemistry ensures chiral purity in the synthesized peptides, making it valuable in pharmaceutical research and development of bioactive peptides. Commonly employed in the production of peptide-based drugs, diagnostics, and biochemical probes.
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