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Structure of 6511-88-2
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2,2,2-Trifluoro-1-(piperazin-1-yl)ethanone delivers a potent trifluoromethyl electrophile paired with a piperazine nitrogen for downstream conjugation. This bench-stable ketone integrates readily into bioactive scaffolds, offering enhanced solubility and metabolic stability in medicinal chemistry applications.
2,2,2-Trifluoro-1-(piperazin-1-yl)ethanone serves as a versatile building block for fluorinated pharmacophores, enabling efficient incorporation of trifluoromethyl and piperazinyl moieties into complex scaffolds. Its bench-stable nature and compatibility with standard coupling reactions facilitate direct functionalization in medicinal chemistry campaigns. The molecule functions effectively in amide bond formation and heterocycle synthesis, offering predictable reactivity and straightforward purification.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H411
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Precautionary Statements : P264-P270-P273-P330-P391-P405-P501
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Lot numbers can be found on the outside label of a product: