tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate
97%
- Product Code: 85244
CAS:
1209780-71-1
| Molecular Weight: | 237.24 g./mol | Molecular Formula: | C₁₀H₁₇F₂NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16250751 | |
| Melting Point: | Boiling Point: | 296.2±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring with hydroxyl and difluoro substituents, makes it valuable for developing compounds with potential therapeutic applications. It is often employed in the preparation of inhibitors targeting enzymes or receptors, particularly in the field of neurology and oncology. The tert-butyl carboxylate group enhances its stability and reactivity, facilitating its use in complex organic transformations. Additionally, it serves as a building block in the creation of novel drug candidates, contributing to advancements in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿684.00 |
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| 0.250 | 10-20 days | ฿1,251.00 |
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| 1.000 | 10-20 days | ฿2,817.00 |
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| 5.000 | 10-20 days | ฿13,887.00 |
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tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring with hydroxyl and difluoro substituents, makes it valuable for developing compounds with potential therapeutic applications. It is often employed in the preparation of inhibitors targeting enzymes or receptors, particularly in the field of neurology and oncology. The tert-butyl carboxylate group enhances its stability and reactivity, facilitating its use in complex organic transformations. Additionally, it serves as a building block in the creation of novel drug candidates, contributing to advancements in medicinal chemistry and drug discovery.
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