(3R,4R)-1-(tert-Butoxycarbonyl)-3-fluoropiperidine-4-carboxylic acid

95%

Reagent Code: #230981
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CAS Number 1864003-59-7

science Other reagents with same CAS 1864003-59-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.26 g/mol
Formula C₁₁H₁₈FNO₄
badge Registry Numbers
MDL Number MFCD28016233
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine ring and free carboxylic acid group, make it valuable in medicinal chemistry for optimizing metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and receptor modulators, especially in programs focused on antiviral and neurodegenerative disease treatments. The Boc-protected amine allows for selective functionalization, enabling stepwise construction of complex molecules in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,320.00
inventory 250mg
10-20 days ฿42,220.00
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(3R,4R)-1-(tert-Butoxycarbonyl)-3-fluoropiperidine-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine ring and free carboxylic acid group, make it valuable in medicinal chemistry for optimizing metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and receptor modulators, especially in programs focused on antiviral and neurode

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine ring and free carboxylic acid group, make it valuable in medicinal chemistry for optimizing metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and receptor modulators, especially in programs focused on antiviral and neurodegenerative disease treatments. The Boc-protected amine allows for selective functionalization, enabling stepwise construction of complex molecules in multi-step syntheses.

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