1-(Tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid
95%
- Product Code: 39580
CAS:
661458-34-0
Molecular Weight: | 265.2538 g./mol | Molecular Formula: | C₁₁H₁₇F₂NO₄ |
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EC Number: | MDL Number: | MFCD13189902 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a difluoropiperidine moiety, makes it valuable in the development of active pharmaceutical ingredients (APIs), particularly in medicinal chemistry. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the piperidine ring. The presence of fluorine atoms enhances the biological activity and metabolic stability of the resulting compounds, making it useful in the design of drugs targeting neurological disorders, cancer, and other therapeutic areas. Additionally, it serves as a building block in peptide synthesis and the creation of novel chemical entities for drug discovery programs.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿8,685.00 |
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1-(Tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a difluoropiperidine moiety, makes it valuable in the development of active pharmaceutical ingredients (APIs), particularly in medicinal chemistry. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the piperidine ring. The presence of fluorine atoms enhances the biological activity and metabolic stability of the resulting compounds, making it useful in the design of drugs targeting neurological disorders, cancer, and other therapeutic areas. Additionally, it serves as a building block in peptide synthesis and the creation of novel chemical entities for drug discovery programs.
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