(S)-5-Methoxy-5-oxo-2-(tritylamino)pentanoic acid

95%

Reagent Code: #236260
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CAS Number 55878-80-3

science Other reagents with same CAS 55878-80-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.47 g/mol
Formula C₂₅H₂₅NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of enzyme inhibitors where stereochemistry plays a critical role in biological activity. Its trityl-protected amine group allows for selective deprotection and coupling in solid-phase peptide synthesis, making it valuable in medicinal chemistry for creating structurally complex, bioactive molecules. The compound is also employed in the preparation of intermediates for protease inhibitors and other therapeutic agents requiring high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,350.00
inventory 250mg
10-20 days ฿3,910.00
inventory 1g
10-20 days ฿7,830.00
(S)-5-Methoxy-5-oxo-2-(tritylamino)pentanoic acid
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Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of enzyme inhibitors where stereochemistry plays a critical role in biological activity. Its trityl-protected amine group allows for selective deprotection and coupling in solid-phase peptide synthesis, making it valuable in medicinal chemistry for creating structurally complex, bioactive molecules. The compound is also employed in the preparation of intermediates for protease inhibitors and

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of enzyme inhibitors where stereochemistry plays a critical role in biological activity. Its trityl-protected amine group allows for selective deprotection and coupling in solid-phase peptide synthesis, making it valuable in medicinal chemistry for creating structurally complex, bioactive molecules. The compound is also employed in the preparation of intermediates for protease inhibitors and other therapeutic agents requiring high enantiomeric purity.

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