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Structure of 360-95-2
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This trifluoromethylated morpholino ketone features a highly electron-deficient carbonyl flanked by a sterically hindered trifluoromethyl group and a polar morpholine ring. The combination imparts enhanced solubility in organic solvents while maintaining bench-stable handling characteristics, enabling direct incorporation into complex synthetic sequences without requiring pre-activation.
2,2,2-Trifluoro-1-morpholinoethan-1-one serves as a versatile fluorinated building block in synthetic organic chemistry, enabling efficient introduction of trifluoromethyl and morpholino functionalities. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate straightforward incorporation into complex molecular architectures. The compound functions as a key intermediate in the synthesis of bioactive molecules and pharmaceutical scaffolds, particularly where enhanced lipophilicity and metabolic stability are required.
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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: