4-Bromo-3-fluorophenylacetonitrile
98%
- Product Code: 81066
CAS:
499983-13-0
| Molecular Weight: | 214.03 g./mol | Molecular Formula: | C₈H₅BrFN |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 279°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the production of pharmaceuticals, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its bromo and fluoro substituents make it a valuable precursor in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are critical in creating complex organic molecules. Additionally, it finds application in agrochemical research for synthesizing compounds with potential pesticidal or herbicidal properties. Its nitrile group also allows for further functionalization, enabling the creation of diverse chemical structures for various industrial and research purposes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to light brown Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $12.30 |
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| 1.000 | 10-20 days | $27.30 |
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| 5.000 | 10-20 days | $90.46 |
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| 25.000 | 10-20 days | $448.51 |
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4-Bromo-3-fluorophenylacetonitrile
This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the production of pharmaceuticals, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its bromo and fluoro substituents make it a valuable precursor in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are critical in creating complex organic molecules. Additionally, it finds application in agrochemical research for synthesizing compounds with potential pesticidal or herbicidal properties. Its nitrile group also allows for further functionalization, enabling the creation of diverse chemical structures for various industrial and research purposes.
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