(S)-Allyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-aminopentanoate hydrochloride
95%
- Product Code: 233222
CAS:
1624272-55-4
| Molecular Weight: | 430.92 g./mol | Molecular Formula: | C₂₃H₂₇ClN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28125559 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection for the alpha-amino group, allowing selective deprotection under mild basic conditions, while the allyl ester protects the carboxylic acid and can be removed selectively in the presence of other protecting groups. The hydrochloride salt enhances stability and solubility during handling. Commonly employed in the stepwise assembly of complex peptides where orthogonal protection strategies are required. Its chiral (S)-configuration ensures stereochemical control in the final peptide product.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | €283.29 |
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| 250mg | 10-20 days | €481.73 |
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(S)-Allyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-aminopentanoate hydrochloride
Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection for the alpha-amino group, allowing selective deprotection under mild basic conditions, while the allyl ester protects the carboxylic acid and can be removed selectively in the presence of other protecting groups. The hydrochloride salt enhances stability and solubility during handling. Commonly employed in the stepwise assembly of complex peptides where orthogonal protection strategies are required. Its chiral (S)-configuration ensures stereochemical control in the final peptide product.
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