diethyl 1-benzyl-3,4-difluoropyrrolidine-3,4-dicarboxylate
93%
- Product Code: 64480
| Molecular Weight: | 341.35 g./mol | Molecular Formula: | C₁₇H₂₁F₂NO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring difluorinated pyrrolidine and benzyl groups, makes it valuable for designing molecules with enhanced biological activity and metabolic stability. It is often employed in the development of enzyme inhibitors, particularly those targeting proteases or kinases, which are crucial in treating diseases like cancer and viral infections. Additionally, its ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization. Its role in medicinal chemistry underscores its importance in advancing therapeutic innovations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow oil |
| PURITY | 92.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿21,000.00 |
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| 1.000 | 10-20 days | ฿54,000.00 |
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diethyl 1-benzyl-3,4-difluoropyrrolidine-3,4-dicarboxylate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring difluorinated pyrrolidine and benzyl groups, makes it valuable for designing molecules with enhanced biological activity and metabolic stability. It is often employed in the development of enzyme inhibitors, particularly those targeting proteases or kinases, which are crucial in treating diseases like cancer and viral infections. Additionally, its ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization. Its role in medicinal chemistry underscores its importance in advancing therapeutic innovations.
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