N-(Tert-Butoxycarbonyl)-L-Methioninol

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Reagent Code: #217477
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CAS Number 51372-93-1

science Other reagents with same CAS 51372-93-1

blur_circular Chemical Specifications

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Weight 235.34 g/mol
Formula C₁₀H₂₁NO₃S
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a protected amino alcohol building block in organic synthesis, particularly in peptide and peptidomimetic drug development. The Boc-protected methioninol derivative serves as a chiral scaffold for introducing methionine-derived structures with controlled stereochemistry. Commonly employed in solid-phase and solution-phase synthesis to construct complex molecules, including pharmaceuticals and bioactive compounds. Its hydroxyl and protected amine functionalities allow sequential coupling reactions, enabling the assembly of multi-component structures. Also utilized in the preparation of enzyme inhibitors and prodrugs where a metabolically labile methionine-like moiety is required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿580.00
inventory 5g
10-20 days ฿1,780.00
inventory 25g
10-20 days ฿6,470.00

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N-(Tert-Butoxycarbonyl)-L-Methioninol
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Used as a protected amino alcohol building block in organic synthesis, particularly in peptide and peptidomimetic drug development. The Boc-protected methioninol derivative serves as a chiral scaffold for introducing methionine-derived structures with controlled stereochemistry. Commonly employed in solid-phase and solution-phase synthesis to construct complex molecules, including pharmaceuticals and bioactive compounds. Its hydroxyl and protected amine functionalities allow sequential coupling reactions

Used as a protected amino alcohol building block in organic synthesis, particularly in peptide and peptidomimetic drug development. The Boc-protected methioninol derivative serves as a chiral scaffold for introducing methionine-derived structures with controlled stereochemistry. Commonly employed in solid-phase and solution-phase synthesis to construct complex molecules, including pharmaceuticals and bioactive compounds. Its hydroxyl and protected amine functionalities allow sequential coupling reactions, enabling the assembly of multi-component structures. Also utilized in the preparation of enzyme inhibitors and prodrugs where a metabolically labile methionine-like moiety is required.

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