5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)PENT-3-EN-2-ONE
97%
- Product Code: 47978
CAS:
1422-36-2
| Molecular Weight: | 206.0858 g./mol | Molecular Formula: | C₆H₄F₆O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09763630 | |
| Melting Point: | Boiling Point: | 165.9 ℃ at 760mmHg | |
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the synthesis of advanced organic compounds, particularly in the pharmaceutical and agrochemical industries. Its unique trifluoromethyl and trifluoroethyl groups make it a valuable building block for creating molecules with enhanced stability and bioactivity. It is often employed in the development of active pharmaceutical ingredients (APIs) where fluorine substitution is desired to improve metabolic stability, bioavailability, or receptor binding affinity. Additionally, it serves as a key intermediate in the production of specialty chemicals, including dyes, coatings, and materials with specific electronic or optical properties. Its reactivity in organic reactions, such as Michael additions or cyclizations, makes it a versatile reagent in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $531.49 |
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| 5.000 | 10-20 days | $1,951.78 |
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5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)PENT-3-EN-2-ONE
This chemical is primarily utilized in the synthesis of advanced organic compounds, particularly in the pharmaceutical and agrochemical industries. Its unique trifluoromethyl and trifluoroethyl groups make it a valuable building block for creating molecules with enhanced stability and bioactivity. It is often employed in the development of active pharmaceutical ingredients (APIs) where fluorine substitution is desired to improve metabolic stability, bioavailability, or receptor binding affinity. Additionally, it serves as a key intermediate in the production of specialty chemicals, including dyes, coatings, and materials with specific electronic or optical properties. Its reactivity in organic reactions, such as Michael additions or cyclizations, makes it a versatile reagent in synthetic chemistry.
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