S-1-Boc-piperidine-3-carboxylic acid
97%
- Product Code: 234231
Alias:
(S)-Boc-Piperidinic Acid Boc-(S)-3-carboxylic acid Piperidinic Acid 1-Boc-L-Piperidinic Acid
CAS:
88495-54-9
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179172 | |
| Melting Point: | 159-162 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of biologically active molecules. Its Boc-protected amine and carboxylic acid functional groups allow for selective reactions, making it ideal for peptide coupling and the construction of complex nitrogen-containing heterocycles. It is frequently employed in the development of central nervous system agents, including antidepressants, antipsychotics, and analgesics. The piperidine scaffold is common in drug discovery due to its favorable pharmacokinetic properties, and this derivative enables efficient introduction of the ring in a stereocontrolled manner. Its stability and ease of handling further support its use in multi-step organic syntheses, particularly in the production of small-molecule therapeutics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $7.79 |
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| 5.000 | 10-20 days | $31.17 |
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| 25.000 | 10-20 days | $109.61 |
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S-1-Boc-piperidine-3-carboxylic acid
Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of biologically active molecules. Its Boc-protected amine and carboxylic acid functional groups allow for selective reactions, making it ideal for peptide coupling and the construction of complex nitrogen-containing heterocycles. It is frequently employed in the development of central nervous system agents, including antidepressants, antipsychotics, and analgesics. The piperidine scaffold is common in drug discovery due to its favorable pharmacokinetic properties, and this derivative enables efficient introduction of the ring in a stereocontrolled manner. Its stability and ease of handling further support its use in multi-step organic syntheses, particularly in the production of small-molecule therapeutics.
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