(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanoic acid

≥95%

Reagent Code: #50251
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CAS Number 266318-79-0

science Other reagents with same CAS 266318-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.41 g/mol
Formula C₂₁H₂₃NO₄
badge Registry Numbers
MDL Number MFCD03095625
thermostat Physical Properties
Boiling Point 563.9±33.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in the field of peptide synthesis. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for the controlled and sequential construction of peptide chains. The compound is particularly valuable in solid-phase peptide synthesis (SPPS), a method widely employed in the production of peptides for research, pharmaceuticals, and biotechnology. Its application ensures precise and efficient peptide assembly, minimizing unwanted side reactions. Additionally, the Fmoc group can be easily removed under mild conditions, making it a versatile tool in the synthesis of complex peptide structures.

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Test Parameter Specification
Appearance White powder
Purity (%) 95-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,889.00
inventory 250mg
10-20 days ฿1,080.00

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanoic acid
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This chemical is primarily used in the field of peptide synthesis. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for the controlled and sequential construction of peptide chains. The compound is particularly valuable in solid-phase peptide synthesis (SPPS), a method widely employed in the production of peptides for research, pharmaceuticals, and biotechnology. Its application ensures precise and efficient peptide assembly, minimizing unwanted side reactions. Additionally, the Fmoc group can be easily removed under mild conditions, making it a versatile tool in the synthesis of complex peptide structures.
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