(R)-2-(1-(tert-Butoxycarbonyl)piperidin-2-yl)acetic acid
98%
- Product Code: 37469
CAS:
351410-32-7
Molecular Weight: | 243.2900 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
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EC Number: | MDL Number: | MFCD06656438 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules with high precision. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization. Additionally, it is employed in the development of peptide-based drugs and enzyme inhibitors, where its chiral center ensures the desired stereochemistry in the final product. Its application extends to research settings for studying receptor interactions and drug delivery mechanisms.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,232.00 |
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(R)-2-(1-(tert-Butoxycarbonyl)piperidin-2-yl)acetic acid
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules with high precision. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization. Additionally, it is employed in the development of peptide-based drugs and enzyme inhibitors, where its chiral center ensures the desired stereochemistry in the final product. Its application extends to research settings for studying receptor interactions and drug delivery mechanisms.
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