1-(3-Chlorophenyl)-2,2,2-trifluoroethanone
97%
- Product Code: 79310
CAS:
321-31-3
| Molecular Weight: | 208.57 g./mol | Molecular Formula: | C₈H₄ClF₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00461896 | |
| Melting Point: | Boiling Point: | 216.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoromethyl group, makes it valuable for introducing fluorine atoms into more complex molecules, which can enhance their biological activity, metabolic stability, and lipophilicity. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) for drugs targeting various therapeutic areas, including central nervous system disorders and infectious diseases. Additionally, it serves as a building block in the development of herbicides and pesticides, where the trifluoromethyl group contributes to improved efficacy and selectivity. Its reactivity also makes it suitable for use in cross-coupling reactions and other advanced chemical transformations in research and industrial settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $54.86 |
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| 5.000 | 10-20 days | $196.43 |
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| 10.000 | 10-20 days | $306.15 |
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1-(3-Chlorophenyl)-2,2,2-trifluoroethanone
This chemical is primarily utilized in organic synthesis as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoromethyl group, makes it valuable for introducing fluorine atoms into more complex molecules, which can enhance their biological activity, metabolic stability, and lipophilicity. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) for drugs targeting various therapeutic areas, including central nervous system disorders and infectious diseases. Additionally, it serves as a building block in the development of herbicides and pesticides, where the trifluoromethyl group contributes to improved efficacy and selectivity. Its reactivity also makes it suitable for use in cross-coupling reactions and other advanced chemical transformations in research and industrial settings.
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