Methyl 3-(4-Cbz-aminophenyl)-4-fluorobenzoate

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Reagent Code: #213383
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CAS Number 1381944-53-1

science Other reagents with same CAS 1381944-53-1

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scatter_plot Molecular Information
Weight 379.4 g/mol
Formula C₂₂H₁₈FNO₄
badge Registry Numbers
MDL Number MFCD22375074
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide-like frameworks, making it valuable in medicinal chemistry for constructing complex molecules with potential antiviral or anticancer activity. The Cbz-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in research settings for designing enzyme inhibitors where fluorinated aromatic systems enhance binding affinity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,390.00

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Methyl 3-(4-Cbz-aminophenyl)-4-fluorobenzoate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide-like frameworks, making it valuable in medicinal chemistry for constructing complex molecules with potential antiviral or anticancer activity. The Cbz-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in research settings for designing enzyme inhibitor
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide-like frameworks, making it valuable in medicinal chemistry for constructing complex molecules with potential antiviral or anticancer activity. The Cbz-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in research settings for designing enzyme inhibitors where fluorinated aromatic systems enhance binding affinity and metabolic stability.
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