(S)-Methyl 2-amino-4-((tert-butoxycarbonyl)amino)butanoate hydrochloride

97%

Reagent Code: #235071
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CAS Number 3350-15-0

science Other reagents with same CAS 3350-15-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.74 g/mol
Formula C₁₀H₂₁ClN₂O₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and ester functionalities allow for selective reactions in peptide coupling and multi-step organic synthesis. Commonly employed in the preparation of enzyme inhibitors where stereochemistry plays a critical role in biological activity. The Boc-protected amine ensures stability during reactions and can be deprotected under mild acidic conditions, making it suitable for solid-phase and solution-phase peptide synthesis. Frequently utilized in research settings for drug discovery, especially in oncology and antiviral therapies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,100.00
inventory 5g
10-20 days ฿4,880.00
inventory 10g
10-20 days ฿9,750.00
inventory 25g
10-20 days ฿24,340.00
(S)-Methyl 2-amino-4-((tert-butoxycarbonyl)amino)butanoate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and ester functionalities allow for selective reactions in peptide coupling and multi-step organic synthesis. Commonly employed in the preparation of enzyme inhibitors where stereochemistry plays a critical role in biological activity. The Boc-protected amine ensures stability during reactions and can be deprotected under

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and ester functionalities allow for selective reactions in peptide coupling and multi-step organic synthesis. Commonly employed in the preparation of enzyme inhibitors where stereochemistry plays a critical role in biological activity. The Boc-protected amine ensures stability during reactions and can be deprotected under mild acidic conditions, making it suitable for solid-phase and solution-phase peptide synthesis. Frequently utilized in research settings for drug discovery, especially in oncology and antiviral therapies.

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