(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(3,5-dimethylisoxazol-4-yl)phenyl)propanoic acid

95%

Reagent Code: #38015
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CAS Number 1381790-25-5

science Other reagents with same CAS 1381790-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 482.52714 g/mol
Formula C₂₉H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD27952474
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a temporary protecting group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. Its structure, incorporating a 3,5-dimethylisoxazole moiety, makes it useful in the development of peptides with specific biological activities or binding properties, particularly in medicinal chemistry and drug discovery. The compound is also employed in the study of enzyme-substrate interactions and the design of enzyme inhibitors. Its unique phenyl and isoxazole groups contribute to its potential application in targeting protein-protein interactions or modulating biological pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,982.00
inventory 1g
10-20 days ฿71,300.00
inventory 100mg
10-20 days ฿18,610.00
inventory 25mg
10-20 days ฿11,200.00
inventory 500mg
10-20 days ฿57,350.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(3,5-dimethylisoxazol-4-yl)phenyl)propanoic acid
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This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a temporary protecting group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. Its structure, incorporating a 3,5-dimethylisoxazole moiety, makes it useful in the development of peptides with specific biological activities or binding properties, particularly in medicinal chemistry and drug discovery. The compound is also employed in the study of enzyme-substrate interactions and the design of enzyme inhibitors. Its unique phenyl and isoxazole groups contribute to its potential application in targeting protein-protein interactions or modulating biological pathways.
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