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Structure of 944904-58-9
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1-(6-(Trifluoromethyl)pyridin-2-yl)ethan-1-one features a trifluoromethyl group at the 6-position of a pyridine ring, enhancing electron-withdrawing character and metabolic stability. This ketone integrates readily into pharmaceutical intermediates, offering high reactivity in nucleophilic addition and coupling reactions under standard conditions.
1-(6-(Trifluoromethyl)pyridin-2-yl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of biologically relevant heterocycles. Its trifluoromethyl-pyridyl ketone motif exhibits enhanced metabolic stability and modulates electronic properties for target engagement. The molecule demonstrates excellent bench stability, facilitates straightforward purification, and participates reliably in standard transformations such as nucleophilic additions, condensations, and coupling reactions within established synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: