1-Boc-4-allyl-4-piperidinecarboxylic Acid
≥97%
- Product Code: 76193
CAS:
426842-70-8
| Molecular Weight: | 269.34 g./mol | Molecular Formula: | C₁₄H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179130 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) and drug candidates. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions to occur at other sites of the molecule, making it valuable in multi-step synthetic processes. Its structure, featuring an allyl group and a carboxylic acid, enables it to participate in various chemical transformations, such as coupling reactions, cyclizations, and functional group modifications. This versatility makes it a useful component in the creation of compounds with potential therapeutic applications, including those targeting neurological disorders, inflammation, and other medical conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,284.00 |
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| 1.000 | 10-20 days | ฿9,450.00 |
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| 5.000 | 10-20 days | ฿39,510.00 |
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1-Boc-4-allyl-4-piperidinecarboxylic Acid
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) and drug candidates. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions to occur at other sites of the molecule, making it valuable in multi-step synthetic processes. Its structure, featuring an allyl group and a carboxylic acid, enables it to participate in various chemical transformations, such as coupling reactions, cyclizations, and functional group modifications. This versatility makes it a useful component in the creation of compounds with potential therapeutic applications, including those targeting neurological disorders, inflammation, and other medical conditions.
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