2-Bromo-4-chloro-1-(difluoromethyl)benzene
95%
- Product Code: 43231
CAS:
1261476-50-9
| Molecular Weight: | 241.4605 g./mol | Molecular Formula: | C₇H₄BrClF₂ |
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| EC Number: | MDL Number: | MFCD18391081 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring both bromine and chlorine substituents along with a difluoromethyl group, makes it a valuable building block for creating molecules with specific biological activities. In pharmaceuticals, it can be incorporated into drug candidates targeting various diseases, leveraging its halogenated aromatic ring to enhance binding affinity or metabolic stability. In agrochemicals, it is utilized in the development of pesticides or herbicides, where the difluoromethyl group can contribute to improved efficacy or environmental persistence. Additionally, it may serve as a reagent in organic synthesis for introducing functional groups or modifying molecular structures in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿24,543.00 |
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2-Bromo-4-chloro-1-(difluoromethyl)benzene
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring both bromine and chlorine substituents along with a difluoromethyl group, makes it a valuable building block for creating molecules with specific biological activities. In pharmaceuticals, it can be incorporated into drug candidates targeting various diseases, leveraging its halogenated aromatic ring to enhance binding affinity or metabolic stability. In agrochemicals, it is utilized in the development of pesticides or herbicides, where the difluoromethyl group can contribute to improved efficacy or environmental persistence. Additionally, it may serve as a reagent in organic synthesis for introducing functional groups or modifying molecular structures in research and industrial applications.
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