(R)-2-((tert-Butoxycarbonyl)amino)-3-((4-methylbenzyl)selanyl)propanoic acid

97%

Reagent Code: #231486
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CAS Number 869646-27-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.32 g/mol
Formula C₁₆H₂₃NO₄Se
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of selenocysteine-containing peptides, this compound enables the study of selenoproteins and their biological functions. Its selenium moiety allows for enhanced redox activity, making it valuable in biochemical research involving antioxidant enzymes like glutathione peroxidase. The Boc-protected amine group ensures selective peptide coupling, facilitating solid-phase peptide synthesis. It is also employed in the development of enzyme mimics and redox-responsive biomaterials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,640.00
inventory 250mg
10-20 days ฿17,200.00
inventory 1g
10-20 days ฿51,930.00
(R)-2-((tert-Butoxycarbonyl)amino)-3-((4-methylbenzyl)selanyl)propanoic acid
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Used as a key intermediate in the synthesis of selenocysteine-containing peptides, this compound enables the study of selenoproteins and their biological functions. Its selenium moiety allows for enhanced redox activity, making it valuable in biochemical research involving antioxidant enzymes like glutathione peroxidase. The Boc-protected amine group ensures selective peptide coupling, facilitating solid-phase peptide synthesis. It is also employed in the development of enzyme mimics and redox-responsive

Used as a key intermediate in the synthesis of selenocysteine-containing peptides, this compound enables the study of selenoproteins and their biological functions. Its selenium moiety allows for enhanced redox activity, making it valuable in biochemical research involving antioxidant enzymes like glutathione peroxidase. The Boc-protected amine group ensures selective peptide coupling, facilitating solid-phase peptide synthesis. It is also employed in the development of enzyme mimics and redox-responsive biomaterials.

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