N-[(2-Methyl-2-propanyl)oxy]carbonyl-3-(methylsulfonyl)-L-valine

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Reagent Code: #50814
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CAS Number 143978-86-3

science Other reagents with same CAS 143978-86-3

blur_circular Chemical Specifications

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Weight 295.4 g/mol
Formula C₁₁H₂₁NO₆S
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

N-[(2-Methyl-2-propanyl)oxy]carbonyl-3-(methylsulfonyl)-L-valine is a specialty protected amino acid derivative used primarily in peptide synthesis. The tert-butoxycarbonyl (Boc) group protects the α-amino group of the 3-(methylsulfonyl)-L-valine, enabling selective activation and coupling of the carboxylic acid during solid-phase or solution-phase peptide assembly. This ensures precise control over the incorporation of the modified valine residue into peptide chains. The methylsulfonyl (mesyl) substituent at the β-position enhances the compound's solubility in organic solvents and provides improved stability under various reaction conditions. It is particularly valuable in the synthesis of modified peptides, peptidomimetics, and peptide-based pharmaceuticals for drug discovery and biochemical research.

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inventory 250mg
10-20 days ฿20,970.00

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N-[(2-Methyl-2-propanyl)oxy]carbonyl-3-(methylsulfonyl)-L-valine
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N-[(2-Methyl-2-propanyl)oxy]carbonyl-3-(methylsulfonyl)-L-valine is a specialty protected amino acid derivative used primarily in peptide synthesis. The tert-butoxycarbonyl (Boc) group protects the α-amino group of the 3-(methylsulfonyl)-L-valine, enabling selective activation and coupling of the carboxylic acid during solid-phase or solution-phase peptide assembly. This ensures precise control over the incorporation of the modified valine residue into peptide chains. The methylsulfonyl (mesyl) substitue

N-[(2-Methyl-2-propanyl)oxy]carbonyl-3-(methylsulfonyl)-L-valine is a specialty protected amino acid derivative used primarily in peptide synthesis. The tert-butoxycarbonyl (Boc) group protects the α-amino group of the 3-(methylsulfonyl)-L-valine, enabling selective activation and coupling of the carboxylic acid during solid-phase or solution-phase peptide assembly. This ensures precise control over the incorporation of the modified valine residue into peptide chains. The methylsulfonyl (mesyl) substituent at the β-position enhances the compound's solubility in organic solvents and provides improved stability under various reaction conditions. It is particularly valuable in the synthesis of modified peptides, peptidomimetics, and peptide-based pharmaceuticals for drug discovery and biochemical research.

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