2-(2,6-dioxopiperidin-3-yl)-4-fluoroisoindoline-1,3-dione
95%
- Product Code: 64504
CAS:
835616-60-9
| Molecular Weight: | 276.22 g./mol | Molecular Formula: | C₁₃H₉FN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 520.9±45.0 °C(Predicted) | |
| Density: | 1.570±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, particularly in the development of novel therapeutic agents. It serves as a key intermediate in the synthesis of small molecule drugs targeting specific proteins involved in disease pathways. Its structure is often incorporated into proteolysis-targeting chimeras (PROTACs), which are designed to degrade disease-causing proteins selectively. Additionally, it has shown potential in the research of anti-inflammatory and anticancer agents due to its ability to modulate biological pathways effectively. Its fluorinated isoindoline moiety enhances its binding affinity and stability, making it a valuable component in drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off white solid |
| PURITY | 94.5-100 |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | $8.40 |
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| 0.100 | 10-20 days | $9.00 |
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| 1.000 | 10-20 days | $19.50 |
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| 10.000 | 10-20 days | $163.52 |
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2-(2,6-dioxopiperidin-3-yl)-4-fluoroisoindoline-1,3-dione
This compound is primarily utilized in the field of medicinal chemistry, particularly in the development of novel therapeutic agents. It serves as a key intermediate in the synthesis of small molecule drugs targeting specific proteins involved in disease pathways. Its structure is often incorporated into proteolysis-targeting chimeras (PROTACs), which are designed to degrade disease-causing proteins selectively. Additionally, it has shown potential in the research of anti-inflammatory and anticancer agents due to its ability to modulate biological pathways effectively. Its fluorinated isoindoline moiety enhances its binding affinity and stability, making it a valuable component in drug discovery and development.
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