N-(7-Bromo-9-oxo-9H-fluoren-2-yl)acetamide
95%
- Product Code: 52472
CAS:
500300-39-0
| Molecular Weight: | 316.15 g./mol | Molecular Formula: | C₁₅H₁₀BrNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 560.8±43.0 °C(Predicted) | |
| Density: | 1.628±0.06 g/cm3(Predicted) | 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 more complex organic compounds. Its structure, featuring a bromo group and an acetamide moiety, makes it particularly useful in cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and advanced materials. Additionally, the fluorenone core of the molecule is often exploited in the development of dyes, pigments, and organic electronic materials due to its unique electronic properties. Researchers also explore its potential in medicinal chemistry for designing novel drug candidates, particularly targeting diseases where fluorenone derivatives have shown biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | $455.87 |
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| 0.005 | 10-20 days | $1,627.74 |
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N-(7-Bromo-9-oxo-9H-fluoren-2-yl)acetamide
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex organic compounds. Its structure, featuring a bromo group and an acetamide moiety, makes it particularly useful in cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and advanced materials. Additionally, the fluorenone core of the molecule is often exploited in the development of dyes, pigments, and organic electronic materials due to its unique electronic properties. Researchers also explore its potential in medicinal chemistry for designing novel drug candidates, particularly targeting diseases where fluorenone derivatives have shown biological activity.
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