(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-(trifluoromethyl)phenyl)butanoic acid

95%

Reagent Code: #50476
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CAS Number 269726-78-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 469.45 g/mol
Formula C₂₆H₂₂F₃NO₄
badge Registry Numbers
MDL Number MFCD01860973
thermostat Physical Properties
Boiling Point 632.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain assembly. The trifluoromethylphenyl moiety enhances the compound's stability and can influence the peptide's biological activity or binding properties. It is commonly employed in the development of pharmaceuticals, especially in the design of peptide-based drugs targeting specific receptors or enzymes. Additionally, it finds applications in research for studying protein-protein interactions and developing bioactive peptides with therapeutic potential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿58,122.00
inventory 100mg
10-20 days ฿3,924.00
inventory 250mg
10-20 days ฿6,327.00
inventory 1g
10-20 days ฿16,173.00
(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-(trifluoromethyl)phenyl)butanoic acid
This compound is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain assembly. The trifluoromethylphenyl moiety enhances the compound's stability and can influence the peptide's biological activity or binding properties. It is commonly employed in the development of pharmaceuticals, especially in the design of peptide-based drugs targeting specific receptors or enzymes. Additionally, it finds applications in research for studying protein-protein interactions and developing bioactive peptides with therapeutic potential.
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