1-(Piperidine-4-carbonyl)piperidin-4-one hydrochloride

97%

Reagent Code: #114502
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CAS Number 1189684-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.73 g/mol
Formula C₁₁H₁₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD05864748
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring both piperidine and carbonyl functional groups, makes it a valuable building block for developing compounds with potential therapeutic effects. It is often employed in the design and synthesis of drug candidates targeting neurological disorders, such as Alzheimer's disease, due to its ability to interact with specific receptors in the brain. Additionally, it is explored for its role in creating inhibitors for enzymes involved in inflammatory pathways, contributing to the development of anti-inflammatory drugs. Its hydrochloride form enhances solubility, making it more suitable for use in experimental and formulation processes. Researchers also investigate its potential in optimizing pharmacokinetic properties of drug molecules, ensuring better bioavailability and efficacy.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $38.60
inventory 1g
10-20 days $99.50
1-(Piperidine-4-carbonyl)piperidin-4-one hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring both piperidine and carbonyl functional groups, makes it a valuable building block for developing compounds with potential therapeutic effects. It is often employed in the design and synthesis of drug candidates targeting neurological disorders, such as Alzheimer's disease, due to its ability to interact with specific receptors in the brain. Additionally, it is explored for its role in creating inhibitors for enzymes involved in inflammatory pathways, contributing to the development of anti-inflammatory drugs. Its hydrochloride form enhances solubility, making it more suitable for use in experimental and formulation processes. Researchers also investigate its potential in optimizing pharmacokinetic properties of drug molecules, ensuring better bioavailability and efficacy.
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