4-Oxo-1,3-piperidinedicarboxylic acid 1-benzyl ester 3-methyl ester
98%
- Product Code: 83878
Alias:
N-CBZ-3-methoxycarbonyl-4-piperidone;
CAS:
159299-93-1
| Molecular Weight: | 291.30 g./mol | Molecular Formula: | C₁₅H₁₇NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 435.2ºC | |
| Density: | 1.266g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate. It plays a significant role in the development of various biologically active molecules, particularly in the synthesis of piperidine-based compounds. Its structure is often exploited in the design of potential drug candidates, especially those targeting neurological and cardiovascular disorders. Additionally, it serves as a building block in the preparation of complex heterocyclic compounds, which are essential in medicinal chemistry for creating molecules with therapeutic properties. Its ester groups make it a versatile reagent for further chemical modifications, enabling the creation of diverse derivatives for pharmacological studies.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| Appearance | WHITE TO LIGHT YELLOW POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $272.39 |
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4-Oxo-1,3-piperidinedicarboxylic acid 1-benzyl ester 3-methyl ester
This compound is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate. It plays a significant role in the development of various biologically active molecules, particularly in the synthesis of piperidine-based compounds. Its structure is often exploited in the design of potential drug candidates, especially those targeting neurological and cardiovascular disorders. Additionally, it serves as a building block in the preparation of complex heterocyclic compounds, which are essential in medicinal chemistry for creating molecules with therapeutic properties. Its ester groups make it a versatile reagent for further chemical modifications, enabling the creation of diverse derivatives for pharmacological studies.
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