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Structure of 130336-16-2
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1-(3,5-Dichlorophenyl)-2,2,2-trifluoroethanone features a trifluoromethyl ketone moiety flanked by electron-withdrawing dichlorophenyl and perfluorinated groups, enabling high reactivity in nucleophilic additions. This bench-stable compound serves as a key electrophilic synthon for constructing fluorinated aromatic scaffolds in medicinal chemistry and materials science.
1-(3,5-Dichlorophenyl)-2,2,2-trifluoroethanone serves as a versatile acylating agent in synthetic organic chemistry, enabling efficient introduction of the trifluoromethyl ketone motif. Its stability under standard bench conditions and compatibility with diverse functional groups facilitate straightforward incorporation into complex molecular architectures, particularly in medicinal chemistry and heterocyclic synthesis 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: