2-Bromo-6-fluoro-4-methylbenzonitrile
97%
- Product Code: 79278
CAS:
1023971-89-2
| Molecular Weight: | 214.03 g./mol | Molecular Formula: | C₈H₅BrFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28503349 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique combination of bromine, fluorine, and nitrile groups makes it particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse aromatic compounds. The fluorine atom can enhance the biological activity and stability of the resulting molecules, making it useful in drug discovery. Additionally, the nitrile group can be transformed into various other functional groups, such as carboxylic acids or amines, expanding its utility in synthetic routes. Its applications are particularly relevant in the development of active pharmaceutical ingredients (APIs) and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft79,609.88 |
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| 0.250 | 10-20 days | Ft159,219.77 |
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2-Bromo-6-fluoro-4-methylbenzonitrile
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique combination of bromine, fluorine, and nitrile groups makes it particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse aromatic compounds. The fluorine atom can enhance the biological activity and stability of the resulting molecules, making it useful in drug discovery. Additionally, the nitrile group can be transformed into various other functional groups, such as carboxylic acids or amines, expanding its utility in synthetic routes. Its applications are particularly relevant in the development of active pharmaceutical ingredients (APIs) and advanced materials.
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