R-()-N-Boc-2-piperidinecarboxylic acid
97%
- Product Code: 65768
Alias:
(+)-N-Boc-(R)-2-piperidinecarboxylic acid (R)-N-Boc-piperidine-2-carboxylic acid (R)-(+)-1-(tert-butoxycarbonyl)-2 -Piperidinecarboxylic acid N-Boc-D-piperidine-2-carboxylic acid Boc-D-Pip-OH
CAS:
28697-17-8
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00237380 | |
| Melting Point: | 116-119 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
R-()-N-Boc-2-piperidinecarboxylic acid is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various biologically active compounds, including chiral drugs and peptide derivatives. The Boc (tert-butoxycarbonyl) protecting group in this compound is crucial for safeguarding the amine functionality during complex synthetic processes, allowing for selective reactions at other sites of the molecule. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure substances, which are essential for developing medications with specific therapeutic effects. This compound is also utilized in the production of agrochemicals and fine chemicals, where its structural properties contribute to the creation of high-performance products.
Product Specification:
| Test | Specification |
|---|---|
| ENANTIOMERIC EXCESS | 96.5 100% |
| Melting point | 116 119? |
| OPTICAL ROTATIONC1 ACETIC ACID | 60.5-66.5 |
| PurityGC | 96.5 100% |
| APPEARANCE | White powder, crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | Ft5,387.05 |
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| 25.000 | 10-20 days | Ft23,487.56 |
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| 100.000 | 10-20 days | Ft87,485.76 |
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R-()-N-Boc-2-piperidinecarboxylic acid
R-()-N-Boc-2-piperidinecarboxylic acid is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various biologically active compounds, including chiral drugs and peptide derivatives. The Boc (tert-butoxycarbonyl) protecting group in this compound is crucial for safeguarding the amine functionality during complex synthetic processes, allowing for selective reactions at other sites of the molecule. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure substances, which are essential for developing medications with specific therapeutic effects. This compound is also utilized in the production of agrochemicals and fine chemicals, where its structural properties contribute to the creation of high-performance products.
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