1'-(tert-Butoxycarbonyl)-[1,4'-bipiperidine]-4-carboxylic acid
95%
- Product Code: 86471
CAS:
201810-59-5
| Molecular Weight: | 312.40 g./mol | Molecular Formula: | C₁₆H₂₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06408960 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Store at room temperature, away from light, dry and sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in the construction of peptide-like compounds or small molecule drugs. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the design of compounds targeting neurological or cardiovascular diseases due to the bipiperidine scaffold, which is known to interact with various biological receptors. Additionally, its carboxylic acid group enables easy conjugation with other molecules, enhancing its utility in drug discovery and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,682.00 |
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| 0.250 | 10-20 days | ฿4,545.00 |
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| 1.000 | 10-20 days | ฿12,249.00 |
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1'-(tert-Butoxycarbonyl)-[1,4'-bipiperidine]-4-carboxylic acid
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in the construction of peptide-like compounds or small molecule drugs. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the design of compounds targeting neurological or cardiovascular diseases due to the bipiperidine scaffold, which is known to interact with various biological receptors. Additionally, its carboxylic acid group enables easy conjugation with other molecules, enhancing its utility in drug discovery and medicinal chemistry.
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