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Structure of 1159982-64-5
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1-(1-Boc-4-piperidyl)-2,2,2-trifluoroethylamine features a trifluoromethylated ethyl linker that enhances metabolic stability and lipophilicity. The Boc-protected piperidine moiety enables straightforward deprotection for downstream functionalization. This scaffold integrates readily into bioactive molecules requiring electron-deficient alkyl chains and improved membrane permeability under standard conditions.
1-(1-Boc-4-piperidyl)-2,2,2-trifluoroethylamine serves as a versatile building block for the synthesis of bioactive molecules, enabling efficient incorporation of trifluoromethylated piperidine motifs. The Boc-protected amine offers bench stability and orthogonal handling, while the trifluoroethyl group provides enhanced metabolic stability and modulated lipophilicity. It functions effectively in standard coupling reactions and facilitates access to complex heterocyclic scaffolds relevant to medicinal chemistry.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: