3-(4-Biphenylyl)-N-Fmoc-L-alanine

95%

Reagent Code: #105070
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CAS Number 199110-64-0

science Other reagents with same CAS 199110-64-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 463.53 g/mol
Formula C₃₀H₂₅NO₄
badge Registry Numbers
MDL Number MFCD00191198
inventory_2 Storage & Handling
Storage 2~8℃, dry, sealed

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for incorporating biphenylalanine derivatives into peptides, which are valuable for studying protein-protein interactions and designing peptide-based drugs. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protecting group for the amine functionality, allowing selective deprotection during the synthesis process. The biphenyl moiety can enhance the stability and binding affinity of peptides, making them useful in developing therapeutic agents or biochemical probes. Additionally, it finds applications in material science for creating functionalized surfaces or polymers with specific properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,458.00
inventory 5g
10-20 days ฿6,264.00

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3-(4-Biphenylyl)-N-Fmoc-L-alanine
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for incorporating biphenylalanine derivatives into peptides, which are valuable for studying protein-protein interactions and designing peptide-based drugs. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protecting group for the amine functionality, allowing selective deprotection during the synthesis process. The biphenyl moiety can enhance the stability and bi

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for incorporating biphenylalanine derivatives into peptides, which are valuable for studying protein-protein interactions and designing peptide-based drugs. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protecting group for the amine functionality, allowing selective deprotection during the synthesis process. The biphenyl moiety can enhance the stability and binding affinity of peptides, making them useful in developing therapeutic agents or biochemical probes. Additionally, it finds applications in material science for creating functionalized surfaces or polymers with specific properties.

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