(2R,4S)-1-Benzyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride
≥95%
- Product Code: 36499
CAS:
489446-77-7
| Molecular Weight: | 314.77 g./mol | Molecular Formula: | C₁₄H₁₉ClN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11101170 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring both amino and ester functional groups, makes it valuable in the creation of biologically active molecules, especially those targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, its chiral nature allows for the production of enantiomerically pure substances, which is critical in the development of drugs with specific efficacy and reduced side effects. The hydrochloride salt form enhances its stability and solubility, facilitating its use in various experimental and manufacturing processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,152.00 |
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| 0.250 | 10-20 days | ฿2,313.00 |
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(2R,4S)-1-Benzyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring both amino and ester functional groups, makes it valuable in the creation of biologically active molecules, especially those targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, its chiral nature allows for the production of enantiomerically pure substances, which is critical in the development of drugs with specific efficacy and reduced side effects. The hydrochloride salt form enhances its stability and solubility, facilitating its use in various experimental and manufacturing processes.
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