(S)-1-Methylpyrrolidine-2-carboxamide
97%
- Product Code: 37980
CAS:
94391-71-6
| Molecular Weight: | 128.1723 g./mol | Molecular Formula: | C₆H₁₂N₂O |
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| EC Number: | MDL Number: | MFCD19206880 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(S)-1-Methylpyrrolidine-2-carboxamide is primarily utilized in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its stereochemistry makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require high specificity and efficacy. This compound is often employed in the development of central nervous system (CNS) drugs, including those targeting neurological disorders such as Parkinson’s disease and Alzheimer’s disease. Additionally, it serves as a building block in the creation of small molecule inhibitors and modulators for therapeutic applications, particularly in the field of medicinal chemistry. Its role in asymmetric synthesis also makes it a key component in the preparation of complex molecules with potential biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $283.31 |
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(S)-1-Methylpyrrolidine-2-carboxamide
(S)-1-Methylpyrrolidine-2-carboxamide is primarily utilized in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its stereochemistry makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require high specificity and efficacy. This compound is often employed in the development of central nervous system (CNS) drugs, including those targeting neurological disorders such as Parkinson’s disease and Alzheimer’s disease. Additionally, it serves as a building block in the creation of small molecule inhibitors and modulators for therapeutic applications, particularly in the field of medicinal chemistry. Its role in asymmetric synthesis also makes it a key component in the preparation of complex molecules with potential biological activity.
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