5-amino-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
95%
- Product Code: 64563
CAS:
191732-76-0
Molecular Weight: | 273.25 g./mol | Molecular Formula: | C₁₃H₁₁N₃O₄ |
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EC Number: | MDL Number: | ||
Melting Point: | >300 °C | Boiling Point: | 603.8±50.0 °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 that target specific proteins involved in disease pathways. Its structural features make it valuable for creating compounds with potential anti-inflammatory, anti-cancer, and immunomodulatory properties. Researchers often incorporate this chemical into drug discovery projects to explore its efficacy in inhibiting protein-protein interactions or modulating enzymatic activity. Additionally, its application extends to the design of proteolysis-targeting chimeras (PROTACs), which are innovative molecules used to degrade disease-causing proteins selectively.
Product Specification:
Test | Specification |
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APPEARANCE | Yellow solid |
PURITY | 94.5-100 |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $74.84 |
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0.250 | 10-20 days | $144.15 |
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1.000 | 10-20 days | $445.00 |
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10.000 | 10-20 days | $1,808.14 |
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5-amino-2-(2,6-dioxopiperidin-3-yl)isoindoline-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 that target specific proteins involved in disease pathways. Its structural features make it valuable for creating compounds with potential anti-inflammatory, anti-cancer, and immunomodulatory properties. Researchers often incorporate this chemical into drug discovery projects to explore its efficacy in inhibiting protein-protein interactions or modulating enzymatic activity. Additionally, its application extends to the design of proteolysis-targeting chimeras (PROTACs), which are innovative molecules used to degrade disease-causing proteins selectively.
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