(R)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide
≥98%
- Product Code: 62502
CAS:
105024-93-9
| Molecular Weight: | 384.48 g./mol | Molecular Formula: | C₂₅H₂₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18910207 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a benzoylphenyl group and a benzylpyrrolidine moiety, makes it a valuable building block for developing compounds with potential therapeutic effects. It is often explored in the design of drugs targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. Additionally, its chiral center allows for the development of enantioselective compounds, which can enhance specificity and reduce side effects in drug candidates. Researchers also investigate its potential in creating novel analgesics or anti-inflammatory agents due to its structural similarity to other bioactive molecules in these categories.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Slightly pale yellow Crystal - Powder |
| PURITY | 97.5-100 |
| Specific rotation 20Dc1 MeOH | 137-+142 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿880.00 |
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| 1.000 | 10-20 days | ฿2,200.00 |
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(R)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a benzoylphenyl group and a benzylpyrrolidine moiety, makes it a valuable building block for developing compounds with potential therapeutic effects. It is often explored in the design of drugs targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. Additionally, its chiral center allows for the development of enantioselective compounds, which can enhance specificity and reduce side effects in drug candidates. Researchers also investigate its potential in creating novel analgesics or anti-inflammatory agents due to its structural similarity to other bioactive molecules in these categories.
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