1-(Piperidine-4-carbonyl)piperidin-4-one hydrochloride
97%
- Product Code: 114502
CAS:
1189684-40-9
| Molecular Weight: | 246.73 g./mol | Molecular Formula: | C₁₁H₁₉ClN₂O₂ |
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| EC Number: | MDL Number: | MFCD05864748 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿970.00 |
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| 1.000 | 10-20 days | ฿2,500.00 |
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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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