(2S,4S)-4-Fluoropyrrolidine-2-carboxamide hydrochloride
98%
- Product Code: 73133
CAS:
426844-23-7
| Molecular Weight: | 168.59 g./mol | Molecular Formula: | C₅H₁₀ClFN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07368567 | |
| Melting Point: | 240 - 245 ℃ | Boiling Point: | 337.3 ℃ at 760 mmHg |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders. Its unique structure, featuring a fluorinated pyrrolidine ring, enhances the pharmacokinetic properties of the resulting drugs, improving their bioavailability and metabolic stability. Researchers often employ it in the development of enzyme inhibitors and receptor modulators, where the fluorine atom plays a critical role in binding affinity and selectivity. Additionally, its hydrochloride form ensures better solubility and handling during synthetic processes, making it a valuable component in the production of potential therapeutic candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $169.49 |
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| 1.000 | 10-20 days | $423.52 |
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(2S,4S)-4-Fluoropyrrolidine-2-carboxamide hydrochloride
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders. Its unique structure, featuring a fluorinated pyrrolidine ring, enhances the pharmacokinetic properties of the resulting drugs, improving their bioavailability and metabolic stability. Researchers often employ it in the development of enzyme inhibitors and receptor modulators, where the fluorine atom plays a critical role in binding affinity and selectivity. Additionally, its hydrochloride form ensures better solubility and handling during synthetic processes, making it a valuable component in the production of potential therapeutic candidates.
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