4-Bromo-1-(fluoromethyl)-2-methylbenzene
97%
- Product Code: 47297
CAS:
1824142-81-5
| Molecular Weight: | 203.05 g./mol | Molecular Formula: | C₈H₈BrF |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22492378 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the production of more complex compounds. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both bromine and fluorine substituents, makes it a versatile reagent in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitrogen bonds. Additionally, it finds application in agrochemical research for the synthesis of novel pesticides or herbicides, leveraging its halogenated aromatic ring for enhanced reactivity and specificity. Its use in material science is also notable, particularly in the design of organic electronic materials or liquid crystals, where its unique electronic properties can be exploited.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,485.00 |
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| 0.250 | 10-20 days | ฿2,475.00 |
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| 1.000 | 10-20 days | ฿7,425.00 |
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4-Bromo-1-(fluoromethyl)-2-methylbenzene
This chemical is primarily used in organic synthesis as an intermediate for the production of more complex compounds. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both bromine and fluorine substituents, makes it a versatile reagent in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitrogen bonds. Additionally, it finds application in agrochemical research for the synthesis of novel pesticides or herbicides, leveraging its halogenated aromatic ring for enhanced reactivity and specificity. Its use in material science is also notable, particularly in the design of organic electronic materials or liquid crystals, where its unique electronic properties can be exploited.
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