tert-Butyl 3-(1-amino-2-methoxy-2-oxoethyl)pyrrolidine-1-carboxylate
≥95%
- Product Code: 51663
CAS:
1135916-70-9
| Molecular Weight: | 258.31 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06410514 | |
| Melting Point: | Boiling Point: | 333.4±12.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, protected from light and stored in an inert gas |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a crucial role in the development of active pharmaceutical ingredients (APIs), especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a pyrrolidine ring and a tert-butyl ester group, makes it a versatile building block for creating molecules with specific biological activities. Additionally, it is utilized in peptide synthesis and medicinal chemistry research to modify and enhance the properties of drug candidates. Its application extends to the production of chiral compounds, where its stereochemistry is leveraged to achieve desired enantioselectivity in drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,662.00 |
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| 0.250 | 10-20 days | ฿8,154.00 |
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| 1.000 | 10-20 days | ฿32,535.00 |
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tert-Butyl 3-(1-amino-2-methoxy-2-oxoethyl)pyrrolidine-1-carboxylate
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a crucial role in the development of active pharmaceutical ingredients (APIs), especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a pyrrolidine ring and a tert-butyl ester group, makes it a versatile building block for creating molecules with specific biological activities. Additionally, it is utilized in peptide synthesis and medicinal chemistry research to modify and enhance the properties of drug candidates. Its application extends to the production of chiral compounds, where its stereochemistry is leveraged to achieve desired enantioselectivity in drug development.
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