(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(7-fluoro-1H-indol-3-yl)propanoic acid

95%

Reagent Code: #38029
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CAS Number 1956434-65-3

science Other reagents with same CAS 1956434-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 444.45 g/mol
Formula C₂₆H₂₁FN₂O₄
badge Registry Numbers
MDL Number MFCD26960591
thermostat Physical Properties
Boiling Point 713.9±60.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. The fluoroindole moiety makes it valuable in the synthesis of peptides with specific biological activities, especially those targeting receptor binding or enzyme inhibition. Its application is crucial in the development of pharmaceuticals, including drug candidates for neurological disorders, cancer, and other diseases where indole derivatives play a significant role. Additionally, it is utilized in research to study peptide structure-activity relationships and to create peptide-based probes for biochemical assays.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,168.00
inventory 250mg
10-20 days ฿24,336.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(7-fluoro-1H-indol-3-yl)propanoic acid
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. The fluoroindole moiety makes it valuable in the synthesis of peptides with specific biological activities, especially those targeting receptor binding or enzyme inhibition. Its application is crucial in the development of pharmaceuticals, including drug candidates for neurological disorders, cancer, and other diseases where indole derivatives play a significant role. Additionally, it is utilized in research to study peptide structure-activity relationships and to create peptide-based probes for biochemical assays.
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