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

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Reagent Code: #38368
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CAS Number 270065-87-7

science Other reagents with same CAS 270065-87-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 426.4600 g/mol
Formula C₂₆H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD01861077
thermostat Physical Properties
Boiling Point 682.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.33g/cm3
Storage -20°C

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amino group, ensuring selective reactions during peptide chain assembly. The presence of the cyano group on the phenyl ring can introduce specific structural or functional properties into the final peptide, such as enhanced binding affinity or stability. It is commonly employed in pharmaceutical research and development for creating peptide-based drugs, biomaterials, and probes for biochemical studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,048.00

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-cyanophenyl)butanoic acid
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This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amino group, ensuring selective reactions during peptide chain assembly. The presence of the cyano group on the phenyl ring can introduce specific structural or functional properties into the final peptide, such as enhanced binding affinity or stability. It is commonly employed in pharmaceutical research and development for creating peptide-based drugs, biomaterials, and probes for biochemical studies.
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