1-Cyclopentyl-2,2,2-trifluoroethan-1-one
95%
- Product Code: 156667
CAS:
101066-63-1
| Molecular Weight: | 166.14 g./mol | Molecular Formula: | C₇H₉OF₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07380747 | |
| Melting Point: | Boiling Point: | 141.2±35.0 °C(Predicted) | |
| Density: | 1.218±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily as a specialty intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both a cyclopentyl group and trifluoromethyl moiety, makes it valuable for constructing fluorinated compounds with enhanced metabolic stability and bioavailability. It serves as a building block in the development of active ingredients where fluorine substitution improves lipophilicity and resistance to oxidative degradation. Commonly employed in the preparation of ketone-based analogs for medicinal chemistry research, including CNS agents and enzyme inhibitors. Its reactivity allows for carbon-carbon bond formation through nucleophilic addition or enolate chemistry, enabling diverse molecular derivatization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,380.00 |
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| 1.000 | 10-20 days | ฿43,040.00 |
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1-Cyclopentyl-2,2,2-trifluoroethan-1-one
Used primarily as a specialty intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both a cyclopentyl group and trifluoromethyl moiety, makes it valuable for constructing fluorinated compounds with enhanced metabolic stability and bioavailability. It serves as a building block in the development of active ingredients where fluorine substitution improves lipophilicity and resistance to oxidative degradation. Commonly employed in the preparation of ketone-based analogs for medicinal chemistry research, including CNS agents and enzyme inhibitors. Its reactivity allows for carbon-carbon bond formation through nucleophilic addition or enolate chemistry, enabling diverse molecular derivatization.
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