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Structure of 2488795-56-6
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(R)-3-(1-Aminoethyl)-5-(trifluoromethyl)aniline (hydrochloride) delivers a chiral, electron-deficient arylamine scaffold with enhanced solubility and stability under standard conditions. This bench-stable derivative integrates readily into asymmetric synthesis workflows, enabling efficient access to bioactive intermediates in medicinal chemistry.
(R)-3-(1-Aminoethyl)-5-(trifluoromethyl)aniline (hydrochloride) serves as a valuable chiral building block for the synthesis of bioactive molecules, leveraging its trifluoromethyl group for enhanced metabolic stability and lipophilicity. The amine functionality enables straightforward derivatization via amidation, alkylation, or reductive amination, while the hydrochloride salt ensures excellent bench stability and ease of handling. This compound functions as a key intermediate in the construction of heterocyclic scaffolds relevant to medicinal chemistry programs.
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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: