5-[(3S,4R)-1-[(Tert-Butoxy)Carbonyl]-3-[(Tert-Butyldimethylsilyl)Oxy]MethylPiperidin-4-Yl]-2-Fluorobenzoic Acid

96%

Reagent Code: #237098
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CAS Number 2055991-10-9

science Other reagents with same CAS 2055991-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 467.65 g/mol
Formula C₂₄H₃₈FNO₅Si
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Its functional groups allow for selective reactions in multi-step organic syntheses, making it valuable in creating complex drug molecules. Commonly employed in research settings for modifying bioactive structures, especially in antiviral and oncology-related drug discovery. The presence of protective groups (Boc and TBS) enables controlled deprotection and coupling steps, ensuring high specificity during peptide or peptidomimetic assembly.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,550.00
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5-[(3S,4R)-1-[(Tert-Butoxy)Carbonyl]-3-[(Tert-Butyldimethylsilyl)Oxy]MethylPiperidin-4-Yl]-2-Fluorobenzoic Acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Its functional groups allow for selective reactions in multi-step organic syntheses, making it valuable in creating complex drug molecules. Commonly employed in research settings for modifying bioactive structures, especially in antiviral and oncology-related drug discovery. The presence of protective groups (Boc and TBS) enables controlled deprotection and coupling steps, ensurin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Its functional groups allow for selective reactions in multi-step organic syntheses, making it valuable in creating complex drug molecules. Commonly employed in research settings for modifying bioactive structures, especially in antiviral and oncology-related drug discovery. The presence of protective groups (Boc and TBS) enables controlled deprotection and coupling steps, ensuring high specificity during peptide or peptidomimetic assembly.

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