N-Boc-piperidine-4-carbonitrile
99%
- Product Code: 51139
Alias:
1-Boc-4-cyanopiperidine
CAS:
91419-52-2
| Molecular Weight: | 210.27 g./mol | Molecular Formula: | C₁₁H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861223 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
N-Boc-piperidine-4-carbonitrile is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various bioactive compounds and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions at other sites, making it valuable in multi-step synthetic processes. It is often employed in the synthesis of piperidine derivatives, which are essential in the development of drugs targeting the central nervous system, including antipsychotics, antidepressants, and analgesics. Additionally, its nitrile functional group provides versatility for further chemical transformations, such as hydrolysis to carboxylic acids or reduction to amines, enabling the creation of diverse molecular structures. Its stability and reactivity make it a preferred choice in medicinal chemistry and drug discovery research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to tan powder |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
| MELTING POINT | 60-63 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $12.04 |
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| 5.000 | 10-20 days | $27.41 |
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| 25.000 | 10-20 days | $82.64 |
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| 100.000 | 10-20 days | $324.76 |
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N-Boc-piperidine-4-carbonitrile
N-Boc-piperidine-4-carbonitrile is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various bioactive compounds and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions at other sites, making it valuable in multi-step synthetic processes. It is often employed in the synthesis of piperidine derivatives, which are essential in the development of drugs targeting the central nervous system, including antipsychotics, antidepressants, and analgesics. Additionally, its nitrile functional group provides versatility for further chemical transformations, such as hydrolysis to carboxylic acids or reduction to amines, enabling the creation of diverse molecular structures. Its stability and reactivity make it a preferred choice in medicinal chemistry and drug discovery research.
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