tert-Butyl 4-(2-ethoxy-2-oxoethyl)-3-fluoropiperidine-1-carboxylate

95%

Reagent Code: #83777
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CAS Number 317360-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.343 g/mol
Formula C₁₄H₂₄FNO₄
badge Registry Numbers
MDL Number MFCD18632740
thermostat Physical Properties
Boiling Point 346.3±27.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.1±0.1 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of more complex chemical structures. Its unique structure, featuring both a fluoropiperidine ring and an ethoxy ester group, makes it valuable for constructing pharmacologically active molecules. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular systems. The fluorine atom enhances the compound's ability to interact with biological targets, while the ester group provides a reactive site for further chemical modifications. Researchers also use it in the study of enzyme inhibition and receptor binding due to its versatile reactivity and stability under various conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $579.69
inventory 250mg
10-20 days $1,043.44
tert-Butyl 4-(2-ethoxy-2-oxoethyl)-3-fluoropiperidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of more complex chemical structures. Its unique structure, featuring both a fluoropiperidine ring and an ethoxy ester group, makes it valuable for constructing pharmacologically active molecules. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular systems. The fluorine atom enhances the compound's ability to interact with biological targets, while the ester group provides a reactive site for further chemical modifications. Researchers also use it in the study of enzyme inhibition and receptor binding due to its versatile reactivity and stability under various conditions.
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