(3S,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate

97%

Reagent Code: #237505
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CAS Number 907544-20-1

science Other reagents with same CAS 907544-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.27 g/mol
Formula C₁₀H₁₉FN₂O₂
badge Registry Numbers
MDL Number MFCD17976872
thermostat Physical Properties
Boiling Point 285.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine ring and protected amine group, make it valuable in medicinal chemistry for enhancing metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and receptor modulators, especially in antiviral and antidepressant drug candidates. The stereochemistry allows for selective interactions with enzyme active sites, improving potency and reducing off-target effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿230.00
inventory 250mg
10-20 days ฿470.00
inventory 1g
10-20 days ฿1,840.00
inventory 5g
10-20 days ฿9,110.00
inventory 10g
10-20 days ฿16,640.00
inventory 25g
10-20 days ฿41,560.00
inventory 50g
10-20 days ฿75,540.00

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(3S,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine ring and protected amine group, make it valuable in medicinal chemistry for enhancing metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and receptor modulators, especially in antiviral and antidepressant drug

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine ring and protected amine group, make it valuable in medicinal chemistry for enhancing metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and receptor modulators, especially in antiviral and antidepressant drug candidates. The stereochemistry allows for selective interactions with enzyme active sites, improving potency and reducing off-target effects.

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