3-Bromo-5-fluorobenzonitrile
98%
- Product Code: 65553
CAS:
179898-34-1
| Molecular Weight: | 200.01 g./mol | Molecular Formula: | C₇H₃BrFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04038227 | |
| Melting Point: | 43 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. Its unique structure, featuring both bromine and fluorine substituents, makes it a valuable intermediate in the pharmaceutical industry for the creation of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce aromatic rings with specific functional groups into target compounds. Additionally, it serves as a precursor in agrochemical research for designing novel pesticides or herbicides. Its electron-withdrawing properties also make it useful in materials science, particularly in the synthesis of organic electronic materials or liquid crystals.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 98-100 |
| APPEARANCE | White to pale yellow powder, crystals and/or chunk |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $11.70 |
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| 5.000 | 10-20 days | $38.70 |
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| 10.000 | 10-20 days | $71.71 |
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3-Bromo-5-fluorobenzonitrile
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. Its unique structure, featuring both bromine and fluorine substituents, makes it a valuable intermediate in the pharmaceutical industry for the creation of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce aromatic rings with specific functional groups into target compounds. Additionally, it serves as a precursor in agrochemical research for designing novel pesticides or herbicides. Its electron-withdrawing properties also make it useful in materials science, particularly in the synthesis of organic electronic materials or liquid crystals.
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