4-(2-Bromoethyl)-1,2-difluorobenzene
95%
- Product Code: 66336
CAS:
175018-77-6
| Molecular Weight: | 221.04 g./mol | Molecular Formula: | C₈H₇BrF₂ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis and pharmaceutical research as a versatile intermediate. Its structure, featuring a bromoethyl group and difluorobenzene ring, makes it valuable for constructing more complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce fluorinated aromatic moieties into target compounds. Additionally, its reactivity allows for further functionalization, enabling the creation of compounds with potential applications in medicinal chemistry, agrochemicals, and materials science. The presence of fluorine atoms can enhance the biological activity, metabolic stability, and lipophilicity of the resulting molecules, making it a useful building block in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,611.00 |
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| 1.000 | 10-20 days | ฿3,897.00 |
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4-(2-Bromoethyl)-1,2-difluorobenzene
This chemical is primarily utilized in organic synthesis and pharmaceutical research as a versatile intermediate. Its structure, featuring a bromoethyl group and difluorobenzene ring, makes it valuable for constructing more complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce fluorinated aromatic moieties into target compounds. Additionally, its reactivity allows for further functionalization, enabling the creation of compounds with potential applications in medicinal chemistry, agrochemicals, and materials science. The presence of fluorine atoms can enhance the biological activity, metabolic stability, and lipophilicity of the resulting molecules, making it a useful building block in drug discovery and development.
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