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Structure of 42452-42-6
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2,2,2-Trifluoro-2'-(trifluoromethyl)acetophenone features a highly electron-deficient aryl ketone core flanked by trifluoromethyl and trifluoroacetyl groups, enhancing reactivity in nucleophilic addition processes. This bench-stable compound integrates readily into synthetic routes requiring strong polarization effects.
2,2,2-Trifluoro-2'-(trifluoromethyl)acetophenone serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of fluorinated heterocycles and pharmaceutical intermediates. Its dual trifluoromethyl and trifluoromethyl ketone functionalities confer high electrophilicity and metabolic stability, facilitating nucleophilic addition and condensation reactions with broad functional group tolerance. The compound exhibits excellent bench stability and ease of purification, making it well-suited for scalable synthesis and medicinal chemistry applications.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: