(S)-tert-Butyl cyclopropyl(piperidin-3-yl)carbamate

≥95%

Reagent Code: #113859
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CAS Number 250275-25-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.34 g/mol
Formula C₁₃H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD21098144
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a piperidine ring and a cyclopropyl group, makes it a valuable building block for developing pharmaceutical agents, particularly those targeting the central nervous system. It is often employed in the preparation of potential drug candidates for neurological disorders, such as Alzheimer's disease or Parkinson's disease, due to its ability to modulate specific receptors or enzymes in the brain. Additionally, its tert-butyl carbamate group provides stability and protection during synthetic processes, enabling efficient multi-step reactions. Researchers also explore its use in creating novel compounds with potential anti-inflammatory or analgesic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $553.07
inventory 250mg
10-20 days $1,105.78
(S)-tert-Butyl cyclopropyl(piperidin-3-yl)carbamate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a piperidine ring and a cyclopropyl group, makes it a valuable building block for developing pharmaceutical agents, particularly those targeting the central nervous system. It is often employed in the preparation of potential drug candidates for neurological disorders, such as Alzheimer's disease or Parkinson's disease, due to its ability to modulate specific receptors or enzymes in the brain. Additionally, its tert-butyl carbamate group provides stability and protection during synthetic processes, enabling efficient multi-step reactions. Researchers also explore its use in creating novel compounds with potential anti-inflammatory or analgesic properties.
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