4-Ethoxy-1,1,1-trifluoro-3-buten-2-one
98%
- Product Code: 46791
CAS:
17129-06-5
| Molecular Weight: | 168.11 g./mol | Molecular Formula: | C₆H₇F₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192131 | |
| Melting Point: | Boiling Point: | 51-53 °C12 mm Hg(lit.) | |
| Density: | 1.18 g/mL at 25 °C(lit.) | Storage Condition: | 2~8℃ |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its unique structure, featuring both an ethoxy group and a trifluoromethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. It is often employed in reactions to introduce trifluoromethylated compounds, which are known for their enhanced stability and bioactivity. Additionally, it serves as a key intermediate in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry. Its reactivity with various nucleophiles and electrophiles allows for the production of diverse chemical entities with potential applications in drug discovery and material science.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| APPEARANCE | Colorless to yellow to yellow-green liquid |
| REFRACTIVE INDEX N20D | 1.406 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿350.00 |
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| 25.000 | 10-20 days | ฿3,310.00 |
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4-Ethoxy-1,1,1-trifluoro-3-buten-2-one
This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its unique structure, featuring both an ethoxy group and a trifluoromethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. It is often employed in reactions to introduce trifluoromethylated compounds, which are known for their enhanced stability and bioactivity. Additionally, it serves as a key intermediate in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry. Its reactivity with various nucleophiles and electrophiles allows for the production of diverse chemical entities with potential applications in drug discovery and material science.
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