2-(1-(tert-Butoxycarbonyl)-4,4-difluoropiperidin-3-yl)acetic acid
95%
- Product Code: 123980
CAS:
1334417-29-6
| Molecular Weight: | 279.28 g./mol | Molecular Formula: | C₁₂H₁₉F₂NO₄ |
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| EC Number: | MDL Number: | MFCD19686745 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a difluoropiperidine moiety, makes it valuable for the development of drug candidates, particularly in the synthesis of protease inhibitors and other biologically active compounds. The Boc group allows for selective deprotection during multi-step synthetic processes, while the difluoropiperidine component can enhance the metabolic stability and bioavailability of the final drug molecule. Additionally, its acetic acid functional group provides a handle for further chemical modifications, enabling the creation of diverse derivatives for medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿15,084.00 |
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| 0.250 | 10-20 days | ฿25,641.00 |
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2-(1-(tert-Butoxycarbonyl)-4,4-difluoropiperidin-3-yl)acetic acid
This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a difluoropiperidine moiety, makes it valuable for the development of drug candidates, particularly in the synthesis of protease inhibitors and other biologically active compounds. The Boc group allows for selective deprotection during multi-step synthetic processes, while the difluoropiperidine component can enhance the metabolic stability and bioavailability of the final drug molecule. Additionally, its acetic acid functional group provides a handle for further chemical modifications, enabling the creation of diverse derivatives for medicinal chemistry research.
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