4-Bromo-2-fluoro-3-methylbenzonitrile
97%
- Product Code: 81342
CAS:
1114546-30-3
| Molecular Weight: | 214.03 g./mol | Molecular Formula: | C₈H₅BrFN |
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| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex chemical structures. Its unique combination of functional groups, including a bromo, fluoro, and nitrile moiety, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The bromine atom facilitates cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The fluorine atom can enhance the biological activity and metabolic stability of the final compounds, making it useful in drug design. Additionally, the nitrile group offers versatility for further chemical transformations, such as hydrolysis or reduction, to yield carboxylic acids or amines, respectively. This compound is also employed in material science for the synthesis of specialized polymers and liquid crystals, where its structural properties contribute to desired material characteristics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $130.07 |
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| 0.250 | 10-20 days | $392.08 |
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4-Bromo-2-fluoro-3-methylbenzonitrile
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex chemical structures. Its unique combination of functional groups, including a bromo, fluoro, and nitrile moiety, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The bromine atom facilitates cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The fluorine atom can enhance the biological activity and metabolic stability of the final compounds, making it useful in drug design. Additionally, the nitrile group offers versatility for further chemical transformations, such as hydrolysis or reduction, to yield carboxylic acids or amines, respectively. This compound is also employed in material science for the synthesis of specialized polymers and liquid crystals, where its structural properties contribute to desired material characteristics.
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