(2S,4S)-1-Boc-2-cyano-4-fluoropyrrolidine
≥97%
- Product Code: 80483
CAS:
426844-76-0
| Molecular Weight: | 214.24 g./mol | Molecular Formula: | C₁₀H₁₅FN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09263600 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(2S,4S)-1-Boc-2-cyano-4-fluoropyrrolidine is primarily used in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of various biologically active compounds, including potential drug candidates. The Boc (tert-butoxycarbonyl) protecting group ensures stability during synthetic processes, while the cyano and fluoro groups contribute to the molecule's reactivity and ability to form diverse chemical structures. This compound is often employed in the construction of pyrrolidine-based scaffolds, which are prevalent in many therapeutic agents targeting conditions such as cancer, neurological disorders, and infectious diseases. Its stereochemistry also makes it valuable for creating enantiomerically pure compounds, enhancing the efficacy and specificity of the final products.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Brown powder |
| PURITY | 97-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,150.00 |
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| 1.000 | 10-20 days | ฿5,400.00 |
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(2S,4S)-1-Boc-2-cyano-4-fluoropyrrolidine
(2S,4S)-1-Boc-2-cyano-4-fluoropyrrolidine is primarily used in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of various biologically active compounds, including potential drug candidates. The Boc (tert-butoxycarbonyl) protecting group ensures stability during synthetic processes, while the cyano and fluoro groups contribute to the molecule's reactivity and ability to form diverse chemical structures. This compound is often employed in the construction of pyrrolidine-based scaffolds, which are prevalent in many therapeutic agents targeting conditions such as cancer, neurological disorders, and infectious diseases. Its stereochemistry also makes it valuable for creating enantiomerically pure compounds, enhancing the efficacy and specificity of the final products.
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