(R)-2-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid

97%

Reagent Code: #230090
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CAS Number 123254-58-0

science Other reagents with same CAS 123254-58-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
badge Registry Numbers
MDL Number MFCD12963786
thermostat Physical Properties
Boiling Point 341.8±25.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its protected amine group (Boc) and free carboxylic acid allow for selective coupling reactions, making it valuable in solid-phase peptide synthesis. The (R)-enantiomer specificity supports stereoselective synthesis, important for drugs where chirality affects biological activity. Commonly employed in the preparation of enzyme inhibitors and bioactive molecules requiring defined stereochemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,424.50
inventory 100mg
10-20 days ฿3,052.50
inventory 250mg
10-20 days ฿4,889.50
(R)-2-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its protected amine group (Boc) and free carboxylic acid allow for selective coupling reactions, making it valuable in solid-phase peptide synthesis. The (R)-enantiomer specificity supports stereoselective synthesis, important for drugs where chirality affects biological activity. Commonly employed in the preparation of enzyme inhibitors and bioactive molecules requiring defined st

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its protected amine group (Boc) and free carboxylic acid allow for selective coupling reactions, making it valuable in solid-phase peptide synthesis. The (R)-enantiomer specificity supports stereoselective synthesis, important for drugs where chirality affects biological activity. Commonly employed in the preparation of enzyme inhibitors and bioactive molecules requiring defined stereochemistry.

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