(S)-2-((Tert-butoxycarbonyl)amino)-3-(2,5-dichlorophenyl)propanoic acid

97%

Reagent Code: #236022
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CAS Number 1213352-71-6

science Other reagents with same CAS 1213352-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.20 g/mol
Formula C₁₄H₁₇Cl₂NO₄
badge Registry Numbers
MDL Number MFCD07372019
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry and functional groups allow for selective coupling reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of peptide-like structures where control over three-dimensional orientation is critical for biological activity. The Boc-protected amine and carboxylic acid groups enable stepwise assembly in solid-phase and solution-phase peptide synthesis. Also utilized in the production of agrochemicals and specialty organic compounds requiring high enantiomeric purity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,390.00
inventory 250mg
10-20 days ฿12,570.00
inventory 1g
10-20 days ฿30,230.00
(S)-2-((Tert-butoxycarbonyl)amino)-3-(2,5-dichlorophenyl)propanoic acid
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry and functional groups allow for selective coupling reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of peptide-like structures where control over three-dimensional orientation is critical for biological activity. The Boc-protected amine and carboxylic acid groups enable stepwise ass

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry and functional groups allow for selective coupling reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of peptide-like structures where control over three-dimensional orientation is critical for biological activity. The Boc-protected amine and carboxylic acid groups enable stepwise assembly in solid-phase and solution-phase peptide synthesis. Also utilized in the production of agrochemicals and specialty organic compounds requiring high enantiomeric purity.

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