6,7-dibromoquinoxaline-2,3(1H,4H)-dione
95%
- Product Code: 57049
CAS:
89891-77-0
| Molecular Weight: | 319.9 g./mol | Molecular Formula: | C₈H₄Br₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD27931818 | |
| Melting Point: | Boiling Point: | ||
| Density: | 2.081±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique dibrominated quinoxaline core makes it particularly valuable in the creation of heterocyclic compounds, which are often employed in pharmaceutical research and drug discovery. Additionally, it serves as a key intermediate in the preparation of various biologically active molecules, including potential therapeutic agents targeting specific enzymes or receptors. Its application extends to material science, where it can be used in the synthesis of organic semiconductors or dyes due to its electron-deficient aromatic system. Researchers also explore its potential in the development of fluorescent probes or sensors, leveraging its structural properties for specific detection purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $368.09 |
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| 0.250 | 10-20 days | $690.17 |
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| 1.000 | 10-20 days | $1,380.34 |
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6,7-dibromoquinoxaline-2,3(1H,4H)-dione
This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique dibrominated quinoxaline core makes it particularly valuable in the creation of heterocyclic compounds, which are often employed in pharmaceutical research and drug discovery. Additionally, it serves as a key intermediate in the preparation of various biologically active molecules, including potential therapeutic agents targeting specific enzymes or receptors. Its application extends to material science, where it can be used in the synthesis of organic semiconductors or dyes due to its electron-deficient aromatic system. Researchers also explore its potential in the development of fluorescent probes or sensors, leveraging its structural properties for specific detection purposes.
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