4,4-Diethoxy-1,1,1-trifluorobut-3-en-2-one

98%

Reagent Code: #179812
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CAS Number 40657-29-2

science Other reagents with same CAS 40657-29-2

blur_circular Chemical Specifications

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Weight 212.17 g/mol
Formula C₈H₁₁F₃O₃
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MDL Number MFCD08273801
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Storage Room temperature

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Used primarily as a fluorinated building block in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals due to its reactive enone and trifluoromethyl functionalities. The presence of ethoxy groups and the trifluoromethyl unit makes it suitable for condensation reactions and nucleophilic additions, enabling the construction of complex fluorinated molecules. It is particularly useful in the development of bioactive compounds where fluorine substitution enhances metabolic stability, lipophilicity, and binding affinity. Its application extends to the synthesis of intermediates for antifungal agents, anti-inflammatory drugs, and functional materials requiring tailored electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,410.00
inventory 250mg
10-20 days ฿6,300.00
inventory 1g
10-20 days ฿15,540.00

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4,4-Diethoxy-1,1,1-trifluorobut-3-en-2-one
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Used primarily as a fluorinated building block in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals due to its reactive enone and trifluoromethyl functionalities. The presence of ethoxy groups and the trifluoromethyl unit makes it suitable for condensation reactions and nucleophilic additions, enabling the construction of complex fluorinated molecules. It is particularly useful in the development of bioactive compounds where fluorine substitution enhance

Used primarily as a fluorinated building block in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals due to its reactive enone and trifluoromethyl functionalities. The presence of ethoxy groups and the trifluoromethyl unit makes it suitable for condensation reactions and nucleophilic additions, enabling the construction of complex fluorinated molecules. It is particularly useful in the development of bioactive compounds where fluorine substitution enhances metabolic stability, lipophilicity, and binding affinity. Its application extends to the synthesis of intermediates for antifungal agents, anti-inflammatory drugs, and functional materials requiring tailored electronic properties.

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