(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid

≥98%

Reagent Code: #38154
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CAS Number 1175973-95-1

science Other reagents with same CAS 1175973-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 443.49 g/mol
Formula C₂₇H₂₅NO₅
badge Registry Numbers
MDL Number MFCD08061623
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly in pharmaceutical research and bioconjugation studies. The compound’s structure allows for precise control over peptide assembly, making it valuable in the synthesis of bioactive peptides and peptidomimetics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,530.00
inventory 250mg
10-20 days ฿2,700.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)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 protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly

This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly in pharmaceutical research and bioconjugation studies. The compound’s structure allows for precise control over peptide assembly, making it valuable in the synthesis of bioactive peptides and peptidomimetics.

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