N6-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N2-((benzyloxy)carbonyl)-L-lysine

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Reagent Code: #59176
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CAS Number 105751-18-6

science Other reagents with same CAS 105751-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 502.56 g/mol
Formula C₂₉H₃₀N₂O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in peptide synthesis, where it serves as a protected form of lysine. The benzyloxycarbonyl (Cbz) group protects the alpha-amino (N2) functionality, while the fluorenylmethoxycarbonyl (Fmoc) group protects the side chain epsilon-amino (N6) functionality. This allows for selective deprotection and coupling reactions during the step-by-step assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the precise construction of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications. Its use ensures high purity and efficiency in synthesizing peptides with specific sequences and structures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿324.00
inventory 1g
10-20 days ฿675.00

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N6-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N2-((benzyloxy)carbonyl)-L-lysine
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This chemical is primarily used in peptide synthesis, where it serves as a protected form of lysine. The benzyloxycarbonyl (Cbz) group protects the alpha-amino (N2) functionality, while the fluorenylmethoxycarbonyl (Fmoc) group protects the side chain epsilon-amino (N6) functionality. This allows for selective deprotection and coupling reactions during the step-by-step assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the precise construction of complex p

This chemical is primarily used in peptide synthesis, where it serves as a protected form of lysine. The benzyloxycarbonyl (Cbz) group protects the alpha-amino (N2) functionality, while the fluorenylmethoxycarbonyl (Fmoc) group protects the side chain epsilon-amino (N6) functionality. This allows for selective deprotection and coupling reactions during the step-by-step assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the precise construction of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications. Its use ensures high purity and efficiency in synthesizing peptides with specific sequences and structures.

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