4-(4-Fluoro-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester

95%

Reagent Code: #83798
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CAS Number 160296-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.36 g/mol
Formula C₁₇H₂₂FNO₃
badge Registry Numbers
MDL Number MFCD04114990
thermostat Physical Properties
Melting Point 80-83 °C
Boiling Point 410.4±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.155±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluoro-benzoyl group and a piperidine ring, makes it valuable for the development of pharmaceutical agents, particularly those targeting neurological disorders and receptor modulation. It is often employed in the preparation of compounds that interact with the central nervous system, such as potential antipsychotics or analgesics. Additionally, its tert-butyl ester group provides stability during synthetic processes, making it a versatile building block in organic synthesis. Researchers also explore its use in creating novel drug candidates with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $46.38
inventory 250mg
10-20 days $81.16
inventory 1g
10-20 days $165.40
4-(4-Fluoro-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluoro-benzoyl group and a piperidine ring, makes it valuable for the development of pharmaceutical agents, particularly those targeting neurological disorders and receptor modulation. It is often employed in the preparation of compounds that interact with the central nervous system, such as potential antipsychotics or analgesics. Additionally, its tert-butyl ester group provides stability during synthetic processes, making it a versatile building block in organic synthesis. Researchers also explore its use in creating novel drug candidates with improved efficacy and selectivity.
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