(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride
97%
- Product Code: 235016
CAS:
201009-98-5
| Molecular Weight: | 418.91 g./mol | Molecular Formula: | C₂₂H₂₇ClN₂O₄ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating lysine residues with orthogonal protection. The Fmoc group allows for mild base-induced deprotection during solid-phase synthesis, while the hydrochloride salt enhances stability and handling. It enables the stepwise construction of peptides with precise sequence control, commonly applied in research laboratories for developing therapeutic peptides, biochemical probes, and diagnostic agents. Its chirality ensures the formation of biologically active peptides with correct stereochemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | ฿1,400.00 |
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| 10g | 10-20 days | ฿2,740.00 |
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| 25g | 10-20 days | ฿6,770.00 |
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(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating lysine residues with orthogonal protection. The Fmoc group allows for mild base-induced deprotection during solid-phase synthesis, while the hydrochloride salt enhances stability and handling. It enables the stepwise construction of peptides with precise sequence control, commonly applied in research laboratories for developing therapeutic peptides, biochemical probes, and diagnostic agents. Its chirality ensures the formation of biologically active peptides with correct stereochemistry.
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