4-Bromo-3-fluorobenzonitrile
≥98.0%
- Product Code: 81352
CAS:
133059-44-6
| Molecular Weight: | 200.01 g./mol | Molecular Formula: | C₇H₃BrFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07782069 | |
| Melting Point: | 54-58 C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, allows it to participate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating complex molecules. Additionally, it is often employed in the development of liquid crystal materials due to its ability to influence molecular alignment and stability. Its nitrile group further enhances its reactivity, making it a valuable building block in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science applications.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 92-96 |
| PurityGC | 98-100 |
| APPEARANCE | OFF-WHITE TO YELLOW SOLID |
| INFRARED SPECTROMETRY | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | €20.58 |
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| 25.000 | 10-20 days | €72.81 |
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| 100.000 | 10-20 days | €252.74 |
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4-Bromo-3-fluorobenzonitrile
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, allows it to participate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating complex molecules. Additionally, it is often employed in the development of liquid crystal materials due to its ability to influence molecular alignment and stability. Its nitrile group further enhances its reactivity, making it a valuable building block in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science applications.
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