tert-Butyl 3-(2-ethoxy-2-oxoethyl)pyrrolidine-1-carboxylate
97%
- Product Code: 65048
CAS:
664364-29-8
| Molecular Weight: | 257.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₄ |
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| EC Number: | MDL Number: | MFCD11977331 | |
| Melting Point: | Boiling Point: | 321.4±15.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both ester and pyrrolidine groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in the construction of nitrogen-containing heterocycles, which are common in drug molecules. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, enabling the controlled modification of specific functional groups. This compound is also used in research settings for the development of novel chemical entities and in medicinal chemistry studies to explore structure-activity relationships.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $195.85 |
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| 5.000 | 10-20 days | $676.51 |
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tert-Butyl 3-(2-ethoxy-2-oxoethyl)pyrrolidine-1-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both ester and pyrrolidine groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in the construction of nitrogen-containing heterocycles, which are common in drug molecules. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, enabling the controlled modification of specific functional groups. This compound is also used in research settings for the development of novel chemical entities and in medicinal chemistry studies to explore structure-activity relationships.
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