2-(Bromomethyl)-1-chloro-3-(trifluoromethyl)benzene
95%
- Product Code: 42008
CAS:
886500-26-1
Molecular Weight: | 273.4800 g./mol | Molecular Formula: | C₈H₅BrClF₃ |
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EC Number: | MDL Number: | MFCD06660232 | |
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 structure, featuring a bromomethyl group, a chloro substituent, and a trifluoromethyl group, makes it a versatile building block for creating molecules with specific biological activities. It is often employed in the development of active pharmaceutical ingredients (APIs) where the trifluoromethyl group can enhance metabolic stability and bioavailability. Additionally, it is utilized in the production of herbicides and pesticides, where the presence of halogen atoms contributes to the compound's effectiveness in targeting pests or weeds. Its reactivity allows for further functionalization, enabling the creation of diverse chemical entities tailored for specific applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,260.00 |
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2-(Bromomethyl)-1-chloro-3-(trifluoromethyl)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 structure, featuring a bromomethyl group, a chloro substituent, and a trifluoromethyl group, makes it a versatile building block for creating molecules with specific biological activities. It is often employed in the development of active pharmaceutical ingredients (APIs) where the trifluoromethyl group can enhance metabolic stability and bioavailability. Additionally, it is utilized in the production of herbicides and pesticides, where the presence of halogen atoms contributes to the compound's effectiveness in targeting pests or weeds. Its reactivity allows for further functionalization, enabling the creation of diverse chemical entities tailored for specific applications.
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