3-Bromo-2-(trifluoromethyl)benzonitrile
97%
- Product Code: 117946
CAS:
1228898-24-5
| Molecular Weight: | 250.02 g./mol | Molecular Formula: | C₈H₃BrF₃N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16606444 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its unique structure, featuring a bromine atom and a trifluoromethyl group on a benzonitrile core, makes it valuable in the pharmaceutical industry for the creation of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce the trifluoromethyl group into target compounds, which can enhance their biological activity and metabolic stability. Additionally, it is used in agrochemical research to develop novel pesticides and herbicides, leveraging the electron-withdrawing properties of the trifluoromethyl group to improve efficacy. Its applications also extend to materials science, where it serves as a building block for advanced polymers and specialty chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,221.00 |
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| 1.000 | 10-20 days | ฿12,663.00 |
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3-Bromo-2-(trifluoromethyl)benzonitrile
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its unique structure, featuring a bromine atom and a trifluoromethyl group on a benzonitrile core, makes it valuable in the pharmaceutical industry for the creation of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce the trifluoromethyl group into target compounds, which can enhance their biological activity and metabolic stability. Additionally, it is used in agrochemical research to develop novel pesticides and herbicides, leveraging the electron-withdrawing properties of the trifluoromethyl group to improve efficacy. Its applications also extend to materials science, where it serves as a building block for advanced polymers and specialty chemicals.
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