(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-methyltetrahydro-2H-pyran-4-yl)acetic acid

98%

Reagent Code: #236640
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CAS Number 1251769-10-4

science Other reagents with same CAS 1251769-10-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.33 g/mol
Formula C₁₃H₂₃NO₅
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 bioactive molecules. Its Boc-protected amine and free carboxylic acid functionalities allow for selective coupling reactions, making it valuable in peptide-based drug design. The 4-methyltetrahydropyran ring provides structural rigidity and influences metabolic stability, enhancing the pharmacokinetic properties of the final compound. Commonly employed in solid-phase and solution-phase synthesis for creating libraries of structurally diverse compounds in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿38,000.00
inventory 250mg
10-20 days ฿123,760.00

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(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-methyltetrahydro-2H-pyran-4-yl)acetic 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 bioactive molecules. Its Boc-protected amine and free carboxylic acid functionalities allow for selective coupling reactions, making it valuable in peptide-based drug design. The 4-methyltetrahydropyran ring provides structural rigidity and influences metabolic stability, enhancing the pharmacokinetic properties of the final compound. Commonly employed in solid-phase and solu
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its Boc-protected amine and free carboxylic acid functionalities allow for selective coupling reactions, making it valuable in peptide-based drug design. The 4-methyltetrahydropyran ring provides structural rigidity and influences metabolic stability, enhancing the pharmacokinetic properties of the final compound. Commonly employed in solid-phase and solution-phase synthesis for creating libraries of structurally diverse compounds in medicinal chemistry research.
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