(2S,4R)-1-(Tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic acid
97%
- Product Code: 76142
CAS:
364750-80-1
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13185988 | |
| Melting Point: | Boiling Point: | 343.2 °C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry, sealed |
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 drugs, especially those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, it is employed in peptide chemistry, where it acts as a building block for constructing peptide chains with specific stereochemistry. Its protective group (tert-butoxycarbonyl) ensures selective reactions during multi-step synthetic processes, enhancing efficiency and yield.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,027.00 |
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| 0.250 | 10-20 days | ฿10,971.00 |
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| 1.000 | 10-20 days | ฿31,365.00 |
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(2S,4R)-1-(Tert-butoxycarbonyl)-4-methylpyrrolidine-2-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 drugs, especially those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, it is employed in peptide chemistry, where it acts as a building block for constructing peptide chains with specific stereochemistry. Its protective group (tert-butoxycarbonyl) ensures selective reactions during multi-step synthetic processes, enhancing efficiency and yield.
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