(R)-tert-Butyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-iodopropanoate
98%
- Product Code: 37425
CAS:
282734-33-2
Molecular Weight: | 493.3300 g./mol | Molecular Formula: | C₂₂H₂₄INO₄ |
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EC Number: | MDL Number: | MFCD11053633 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the construction of complex peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, preventing unwanted reactions during peptide chain assembly. The tert-butyl ester group protects the carboxyl group, ensuring selective deprotection and coupling steps. The iodine atom in the structure provides a reactive site for further functionalization or cross-coupling reactions, making it valuable in the synthesis of modified peptides or peptide-based compounds. Its application is crucial in pharmaceutical research, particularly in the development of peptide drugs, bioactive peptides, and peptidomimetics.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | £129.26 |
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(R)-tert-Butyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-iodopropanoate
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the construction of complex peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, preventing unwanted reactions during peptide chain assembly. The tert-butyl ester group protects the carboxyl group, ensuring selective deprotection and coupling steps. The iodine atom in the structure provides a reactive site for further functionalization or cross-coupling reactions, making it valuable in the synthesis of modified peptides or peptide-based compounds. Its application is crucial in pharmaceutical research, particularly in the development of peptide drugs, bioactive peptides, and peptidomimetics.
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