1-(3,5-Bis(trifluoromethyl)phenyl)-2-bromoethanone
95%
- Product Code: 63763
CAS:
131805-94-2
| Molecular Weight: | 335.04 g./mol | Molecular Formula: | C₁₀H₅BrF₆O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00792434 | |
| Melting Point: | Boiling Point: | 211.6±35.0 °C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, avoid light, store in inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly as a key intermediate in the production of pharmaceuticals and agrochemicals. Its trifluoromethyl groups enhance the reactivity and stability of the compounds derived from it, making it valuable in the development of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create complex molecules with potential therapeutic properties. Additionally, its bromoethanone moiety allows for further functionalization, enabling the synthesis of diverse chemical structures. In agrochemical research, it contributes to the development of novel pesticides and herbicides by serving as a building block for active compounds. Its unique structure also makes it useful in material science, particularly in the creation of specialty polymers and coatings with enhanced properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | colorless to yellow solid or liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,090.00 |
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| 1.000 | 10-20 days | ฿3,280.00 |
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| 5.000 | 10-20 days | ฿11,480.00 |
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1-(3,5-Bis(trifluoromethyl)phenyl)-2-bromoethanone
This chemical is primarily utilized in organic synthesis, particularly as a key intermediate in the production of pharmaceuticals and agrochemicals. Its trifluoromethyl groups enhance the reactivity and stability of the compounds derived from it, making it valuable in the development of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create complex molecules with potential therapeutic properties. Additionally, its bromoethanone moiety allows for further functionalization, enabling the synthesis of diverse chemical structures. In agrochemical research, it contributes to the development of novel pesticides and herbicides by serving as a building block for active compounds. Its unique structure also makes it useful in material science, particularly in the creation of specialty polymers and coatings with enhanced properties.
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