1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone
≥95%
- Product Code: 117274
CAS:
1190865-44-1
| Molecular Weight: | 261.00 g./mol | Molecular Formula: | C₈H₂Cl₂F₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23382507 | |
| Melting Point: | Boiling Point: | 282.5±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a building block or intermediate in the production of more complex chemical entities. Its unique structure, featuring both chloro and fluoro substituents, makes it valuable in the development of pharmaceuticals and agrochemicals. The trifluoroethanone moiety is often leveraged for its electron-withdrawing properties, which can enhance the reactivity of adjacent functional groups in synthetic pathways. Additionally, the presence of halogen atoms allows for further functionalization through substitution reactions, enabling the creation of diverse derivatives with potential biological activity. Its application is also seen in materials science, where it can be used to synthesize specialized polymers or coatings with specific properties such as chemical resistance or thermal stability.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Liquid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿640.00 |
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| 5.000 | 10-20 days | ฿2,930.00 |
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| 10.000 | 10-20 days | ฿4,880.00 |
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1-(3,5-Dichloro-4-fluorophenyl)-2,2,2-trifluoroethanone
This compound is primarily utilized in the field of organic synthesis, particularly as a building block or intermediate in the production of more complex chemical entities. Its unique structure, featuring both chloro and fluoro substituents, makes it valuable in the development of pharmaceuticals and agrochemicals. The trifluoroethanone moiety is often leveraged for its electron-withdrawing properties, which can enhance the reactivity of adjacent functional groups in synthetic pathways. Additionally, the presence of halogen atoms allows for further functionalization through substitution reactions, enabling the creation of diverse derivatives with potential biological activity. Its application is also seen in materials science, where it can be used to synthesize specialized polymers or coatings with specific properties such as chemical resistance or thermal stability.
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