tert-Butyl 5,5-difluoro-2-(hydroxymethyl)piperidine-1-carboxylate
98%
- Product Code: 85472
CAS:
1255666-39-7
| Molecular Weight: | 251.27 g./mol | Molecular Formula: | C₁₁H₁₉F₂NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18433649 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of complex molecules. Its structure, featuring both difluoro and hydroxymethyl groups, makes it valuable for constructing piperidine-based compounds, which are often found in bioactive molecules and drug candidates. It is particularly useful in the synthesis of potential therapeutic agents targeting neurological disorders, inflammation, or infectious diseases. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, allowing for selective reactions and easier purification. Researchers also employ it in the study of fluorine-containing compounds, leveraging the unique properties of fluorine to improve drug efficacy and metabolic stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,810.00 |
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| 0.250 | 10-20 days | ฿16,668.00 |
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| 1.000 | 10-20 days | ฿45,000.00 |
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tert-Butyl 5,5-difluoro-2-(hydroxymethyl)piperidine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of complex molecules. Its structure, featuring both difluoro and hydroxymethyl groups, makes it valuable for constructing piperidine-based compounds, which are often found in bioactive molecules and drug candidates. It is particularly useful in the synthesis of potential therapeutic agents targeting neurological disorders, inflammation, or infectious diseases. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, allowing for selective reactions and easier purification. Researchers also employ it in the study of fluorine-containing compounds, leveraging the unique properties of fluorine to improve drug efficacy and metabolic stability.
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