(R)-tert-Butyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-iodopropanoate

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Reagent Code: #37425
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CAS Number 282734-33-2

science Other reagents with same CAS 282734-33-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 493.3300 g/mol
Formula C₂₂H₂₄INO₄
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MDL Number MFCD11053633
inventory_2 Storage & Handling
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description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,120.00
inventory 250mg
10-20 days ฿2,770.00

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(R)-tert-Butyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-iodopropanoate
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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 s

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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