(S)-tert-Butyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochloride

97%

Reagent Code: #232982
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CAS Number 197358-53-5

science Other reagents with same CAS 197358-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.79 g/mol
Formula C₁₂H₂₅ClN₂O₄
badge Registry Numbers
MDL Number MFCD30475900
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of peptide-based drugs. Its protected amino and amine functionalities allow selective coupling reactions, making it valuable in solid-phase peptide synthesis. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. The Boc-protected amine ensures stability during reactions and can be easily deprotected under mild acidic conditions, enabling efficient stepwise assembly of complex peptides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,410.00
inventory 25g
10-20 days ฿25,860.00
inventory 1g
10-20 days ฿40,000.00
inventory 100g
10-20 days ฿85,310.00
(S)-tert-Butyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of peptide-based drugs. Its protected amino and amine functionalities allow selective coupling reactions, making it valuable in solid-phase peptide synthesis. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. The Boc-protected amine ensures stability during reactions and can be easily deprotected under mild acidic conditions, enabl

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of peptide-based drugs. Its protected amino and amine functionalities allow selective coupling reactions, making it valuable in solid-phase peptide synthesis. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. The Boc-protected amine ensures stability during reactions and can be easily deprotected under mild acidic conditions, enabling efficient stepwise assembly of complex peptides.

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