(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((4-methoxybenzyl)selanyl)butanoic acid

97%

Reagent Code: #236805
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CAS Number 2044704-59-6

science Other reagents with same CAS 2044704-59-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 524.47 g/mol
Formula C₂₇H₂₇NO₅Se
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in peptide synthesis as a protected selenocysteine derivative, enabling the incorporation of selenium-containing amino acids into peptides for structural and functional studies. The Fmoc group allows for solid-phase synthesis, while the 4-methoxybenzyl selenoether protects the selenium functionality during assembly. After chain assembly, the protecting group can be selectively removed to enable formation of selenol groups or selenide bridges, useful in designing redox-active peptides, enzyme mimics, and stable peptide structures through Se–Se bonds. Also applied in the development of selenopeptides with potential antioxidant or catalytic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,720.00
inventory 250mg
10-20 days ฿39,410.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((4-methoxybenzyl)selanyl)butanoic acid
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Used in peptide synthesis as a protected selenocysteine derivative, enabling the incorporation of selenium-containing amino acids into peptides for structural and functional studies. The Fmoc group allows for solid-phase synthesis, while the 4-methoxybenzyl selenoether protects the selenium functionality during assembly. After chain assembly, the protecting group can be selectively removed to enable formation of selenol groups or selenide bridges, useful in designing redox-active peptides, enzyme mimics,

Used in peptide synthesis as a protected selenocysteine derivative, enabling the incorporation of selenium-containing amino acids into peptides for structural and functional studies. The Fmoc group allows for solid-phase synthesis, while the 4-methoxybenzyl selenoether protects the selenium functionality during assembly. After chain assembly, the protecting group can be selectively removed to enable formation of selenol groups or selenide bridges, useful in designing redox-active peptides, enzyme mimics, and stable peptide structures through Se–Se bonds. Also applied in the development of selenopeptides with potential antioxidant or catalytic properties.

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