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Structure of 340-07-8
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2,2,2-Trifluoro-1-(piperidin-1-yl)ethan-1-one serves as a versatile acylating agent in synthetic organic chemistry, enabling efficient introduction of trifluoromethyl ketone motifs. Its reactivity facilitates nucleophilic acyl substitution with amines and alcohols under mild conditions, offering excellent functional group tolerance and bench stability. The piperidine moiety enhances solubility and supports downstream transformations, making it valuable for constructing fluorinated heterocycles and medicinal chemistry scaffolds.
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GHS Pictogram :
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GHS No : GHS06,GHS09
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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 : H300-H319-H400
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Precautionary Statements : P264-P270-P273-P280-P330-P391-P405-P501
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Lot numbers can be found on the outside label of a product: