4-Bromo-2-(methylsulfonyl)benzonitrile
95%
- Product Code: 81340
CAS:
1208402-11-2
| Molecular Weight: | 260.11 g./mol | Molecular Formula: | C₈H₆BrNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12828670 | |
| Melting Point: | Boiling Point: | 444.7±45.0 °C(Predicted) | |
| Density: | 1.74±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a bromo and methylsulfonyl group, makes it valuable for constructing complex organic frameworks, particularly in the design of potential drug candidates. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic or heteroaromatic moieties into target molecules. Additionally, its nitrile group can be further modified into other functional groups, such as carboxylic acids or amides, enhancing its versatility in medicinal chemistry. This chemical is also explored in material science for the development of organic semiconductors and advanced polymers due to its electron-withdrawing properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $105.83 |
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| 1.000 | 10-20 days | $299.07 |
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4-Bromo-2-(methylsulfonyl)benzonitrile
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a bromo and methylsulfonyl group, makes it valuable for constructing complex organic frameworks, particularly in the design of potential drug candidates. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic or heteroaromatic moieties into target molecules. Additionally, its nitrile group can be further modified into other functional groups, such as carboxylic acids or amides, enhancing its versatility in medicinal chemistry. This chemical is also explored in material science for the development of organic semiconductors and advanced polymers due to its electron-withdrawing properties.
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