Ethyl 2-(4-Oxopiperidin-1-Yl)Acetate
95%
- Product Code: 82329
CAS:
145729-10-8
| Molecular Weight: | 185.22 g./mol | Molecular Formula: | C₉H₁₅NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09936102 | |
| Melting Point: | Boiling Point: | 289.4±25.0 °C(Predicted) | |
| Density: | 1.101±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and bioactive molecules. Its structure, featuring a piperidine ring and an ester group, makes it valuable in the development of drugs targeting neurological and cardiovascular disorders. It is often employed in the synthesis of compounds with potential analgesic, anti-inflammatory, or antihypertensive properties. Additionally, it serves as a building block in the creation of complex molecules for research in medicinal chemistry, particularly in the design of enzyme inhibitors or receptor modulators. Its versatility in chemical reactions, such as ester hydrolysis or nucleophilic substitution, allows for its use in diverse synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,148.00 |
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| 0.250 | 10-20 days | ฿9,360.00 |
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| 1.000 | 10-20 days | ฿18,720.00 |
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Ethyl 2-(4-Oxopiperidin-1-Yl)Acetate
This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and bioactive molecules. Its structure, featuring a piperidine ring and an ester group, makes it valuable in the development of drugs targeting neurological and cardiovascular disorders. It is often employed in the synthesis of compounds with potential analgesic, anti-inflammatory, or antihypertensive properties. Additionally, it serves as a building block in the creation of complex molecules for research in medicinal chemistry, particularly in the design of enzyme inhibitors or receptor modulators. Its versatility in chemical reactions, such as ester hydrolysis or nucleophilic substitution, allows for its use in diverse synthetic pathways.
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