1-Bromo-2-chloro-3-fluoro-4-(trifluoromethyl)benzene
≥95%
- Product Code: 59523
CAS:
1260890-50-3
| Molecular Weight: | 277.44 g./mol | Molecular Formula: | C₇H₂BrClF₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13195463 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, featuring multiple halogen substituents, makes it valuable for introducing specific functional groups into complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting molecules, which is crucial in drug development. In agrochemical research, it serves as a building block for designing herbicides, fungicides, and insecticides with improved efficacy and selectivity. Its versatility also extends to material science, where it is used in the synthesis of advanced polymers and specialty chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,548.00 |
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| 0.250 | 10-20 days | ฿3,654.00 |
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| 1.000 | 10-20 days | ฿13,680.00 |
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1-Bromo-2-chloro-3-fluoro-4-(trifluoromethyl)benzene
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, featuring multiple halogen substituents, makes it valuable for introducing specific functional groups into complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting molecules, which is crucial in drug development. In agrochemical research, it serves as a building block for designing herbicides, fungicides, and insecticides with improved efficacy and selectivity. Its versatility also extends to material science, where it is used in the synthesis of advanced polymers and specialty chemicals.
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