Fmoc-L-2-carbamoylphenylalanine

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Reagent Code: #105064
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CAS Number 959583-60-9

science Other reagents with same CAS 959583-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.45 g/mol
Formula C₂₅H₂₂N₂O₅
badge Registry Numbers
MDL Number MFCD06659143
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Fmoc-L-2-carbamoylphenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The carbamoyl group on the phenylalanine side chain can be involved in specific interactions or further modifications, making it valuable in the synthesis of complex peptides or peptidomimetics. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein-protein interactions. Additionally, it is utilized in the preparation of peptide-based materials and in the exploration of novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿4,950.00

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Fmoc-L-2-carbamoylphenylalanine
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Fmoc-L-2-carbamoylphenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The carbamoyl group on the phenylalanine side chain can be involved in specific interactions or further modifications, making it

Fmoc-L-2-carbamoylphenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The carbamoyl group on the phenylalanine side chain can be involved in specific interactions or further modifications, making it valuable in the synthesis of complex peptides or peptidomimetics. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein-protein interactions. Additionally, it is utilized in the preparation of peptide-based materials and in the exploration of novel therapeutic agents.

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