Methyl 1-Cbz-3-isopropylpiperidine-3-carboxylate
≥97%
- Product Code: 76211
CAS:
1363166-34-0
| Molecular Weight: | 319.40 g./mol | Molecular Formula: | C₁₈H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21641319 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various active pharmaceutical ingredients (APIs) and drug candidates. Its structure, featuring a carboxybenzyl (Cbz) protecting group and an isopropyl piperidine moiety, makes it valuable for constructing nitrogen-containing heterocycles, which are common in many therapeutic agents. Additionally, it is utilized in medicinal chemistry research for the development of compounds targeting neurological disorders, as the piperidine scaffold is often found in drugs affecting the central nervous system. Its ester group also allows for further functionalization, enabling the creation of diverse molecular architectures.
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-Cbz-3-isopropylpiperidine-3-carboxylate
This chemical is primarily used in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various active pharmaceutical ingredients (APIs) and drug candidates. Its structure, featuring a carboxybenzyl (Cbz) protecting group and an isopropyl piperidine moiety, makes it valuable for constructing nitrogen-containing heterocycles, which are common in many therapeutic agents. Additionally, it is utilized in medicinal chemistry research for the development of compounds targeting neurological disorders, as the piperidine scaffold is often found in drugs affecting the central nervous system. Its ester group also allows for further functionalization, enabling the creation of diverse molecular architectures.
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