Fmoc-Lys(Boc)-COCH2Cl
98%
- Product Code: 189596
CAS:
625090-55-3
| Molecular Weight: | 5011 g./mol | Molecular Formula: | C₂₇H₃₃ClN₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in solid-phase peptide synthesis as an activated building block for introducing lysine derivatives with orthogonal protection. The Fmoc group allows for mild base deprotection during stepwise synthesis, while the Boc group remains stable under these conditions, enabling selective deprotection later. The chloroacetyl moiety acts as an electrophilic handle for post-synthetic modifications, such as conjugation to thiols in cysteine-containing peptides or biomolecules. Commonly employed in the preparation of peptide-drug conjugates, cyclic peptides, and bioconjugates for pharmaceutical and biochemical research. Its reactivity facilitates site-specific labeling and crosslinking in complex molecular architectures.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿16,340.00 |
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Fmoc-Lys(Boc)-COCH2Cl
Used in solid-phase peptide synthesis as an activated building block for introducing lysine derivatives with orthogonal protection. The Fmoc group allows for mild base deprotection during stepwise synthesis, while the Boc group remains stable under these conditions, enabling selective deprotection later. The chloroacetyl moiety acts as an electrophilic handle for post-synthetic modifications, such as conjugation to thiols in cysteine-containing peptides or biomolecules. Commonly employed in the preparation of peptide-drug conjugates, cyclic peptides, and bioconjugates for pharmaceutical and biochemical research. Its reactivity facilitates site-specific labeling and crosslinking in complex molecular architectures.
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