(S)-2-Benzyl-3-((tert-butoxycarbonyl)amino)propanoic acid

95%

Reagent Code: #235109
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CAS Number 189619-55-4

science Other reagents with same CAS 189619-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.33 g/mol
Formula C₁₅H₂₁NO₄
badge Registry Numbers
MDL Number MFCD07372495
thermostat Physical Properties
Melting Point 92-100°C
Boiling Point 441.3°C
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 peptides. Its protected amine and carboxylic acid groups allow for selective coupling reactions, making it valuable in solid-phase and solution-phase peptide synthesis. The benzyl side chain provides structural similarity to phenylalanine, enabling its use in designing enzyme inhibitors and receptor ligands. Commonly employed in the preparation of intermediates for drugs targeting viral infections, cardiovascular diseases, and metabolic disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,780.00
inventory 250mg
10-20 days ฿13,560.00
inventory 1g
10-20 days ฿33,760.00
inventory 500mg
10-20 days ฿17,460.00
(S)-2-Benzyl-3-((tert-butoxycarbonyl)amino)propanoic acid
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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 peptides. Its protected amine and carboxylic acid groups allow for selective coupling reactions, making it valuable in solid-phase and solution-phase peptide synthesis. The benzyl side chain provides structural similarity to phenylalanine, enabling its use in designing enzyme inhibitors and receptor ligands. Commonly employed in the preparation of intermed
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active peptides. Its protected amine and carboxylic acid groups allow for selective coupling reactions, making it valuable in solid-phase and solution-phase peptide synthesis. The benzyl side chain provides structural similarity to phenylalanine, enabling its use in designing enzyme inhibitors and receptor ligands. Commonly employed in the preparation of intermediates for drugs targeting viral infections, cardiovascular diseases, and metabolic disorders.
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