trans-1-(tert-Butoxycarbonyl)-4-(ethoxycarbonyl)pyrrolidine-3-carboxylic acid
95%
- Product Code: 105718
CAS:
252919-44-1
| Molecular Weight: | 287.31 g./mol | Molecular Formula: | C₁₃H₂₁NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09608021 | |
| Melting Point: | Boiling Point: | 405.4±45.0 °C(Predicted) | |
| Density: | 1.231±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure, featuring both tert-butoxycarbonyl and ethoxycarbonyl groups, makes it valuable for protecting amine functionalities during multi-step synthetic processes. Additionally, it is employed in the development of peptidomimetics and other molecules that mimic peptide structures, which are crucial in drug discovery for targeting specific biological pathways. Its versatility also extends to the field of medicinal chemistry, where it aids in the creation of compounds with improved pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $276.07 |
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| 0.250 | 10-20 days | $552.14 |
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| 1.000 | 10-20 days | $1,104.27 |
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trans-1-(tert-Butoxycarbonyl)-4-(ethoxycarbonyl)pyrrolidine-3-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure, featuring both tert-butoxycarbonyl and ethoxycarbonyl groups, makes it valuable for protecting amine functionalities during multi-step synthetic processes. Additionally, it is employed in the development of peptidomimetics and other molecules that mimic peptide structures, which are crucial in drug discovery for targeting specific biological pathways. Its versatility also extends to the field of medicinal chemistry, where it aids in the creation of compounds with improved pharmacokinetic properties.
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