Methyl 1-Boc-3-isopropylpiperidine-3-carboxylate
≥97%
- Product Code: 76182
CAS:
1363166-18-0
| Molecular Weight: | 285.38 g./mol | Molecular Formula: | C₁₅H₂₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21641316 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is often employed in the pharmaceutical industry for the preparation of active pharmaceutical ingredients (APIs) or drug candidates. The presence of the Boc (tert-butoxycarbonyl) group makes it a valuable protecting group for amines, allowing selective reactions to occur at other functional sites. Its isopropyl and ester groups contribute to its versatility in constructing piperidine-based compounds, which are common structural motifs in medicinal chemistry. Additionally, it can be used in the synthesis of agrochemicals or fine chemicals, where its unique structure aids in the creation of target molecules with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿9,054.00 |
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| 5.000 | 10-20 days | ฿23,229.00 |
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Methyl 1-Boc-3-isopropylpiperidine-3-carboxylate
This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is often employed in the pharmaceutical industry for the preparation of active pharmaceutical ingredients (APIs) or drug candidates. The presence of the Boc (tert-butoxycarbonyl) group makes it a valuable protecting group for amines, allowing selective reactions to occur at other functional sites. Its isopropyl and ester groups contribute to its versatility in constructing piperidine-based compounds, which are common structural motifs in medicinal chemistry. Additionally, it can be used in the synthesis of agrochemicals or fine chemicals, where its unique structure aids in the creation of target molecules with specific biological activities.
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