(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-fluorophenyl)butanoic acid

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Reagent Code: #38367
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CAS Number 270596-49-1

science Other reagents with same CAS 270596-49-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 419.4500 g/mol
Formula C₂₅H₂₂FNO₄
badge Registry Numbers
MDL Number MFCD01861009
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the synthesis process. Its incorporation allows for the controlled assembly of peptides, particularly in solid-phase peptide synthesis (SPPS). The presence of the 2-fluorophenyl group can influence the peptide's biological activity or stability, making it valuable in the development of pharmaceuticals or bioactive peptides. Additionally, its structure is tailored for applications in medicinal chemistry, where it may be used to create analogs for drug discovery or to study structure-activity relationships.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,520.00

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-fluorophenyl)butanoic acid
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This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the synthesis process. Its incorporation allows for the controlled assembly of peptides, particularly in solid-phase peptide synthesis (SPPS). The presence of the 2-fluorophenyl group can influence the peptide's biological activity or stability, maki

This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the synthesis process. Its incorporation allows for the controlled assembly of peptides, particularly in solid-phase peptide synthesis (SPPS). The presence of the 2-fluorophenyl group can influence the peptide's biological activity or stability, making it valuable in the development of pharmaceuticals or bioactive peptides. Additionally, its structure is tailored for applications in medicinal chemistry, where it may be used to create analogs for drug discovery or to study structure-activity relationships.

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