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Structure of 101396-91-2
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This chiral quaternary ammonium salt features a (S)-configured stereocenter adjacent to a reactive hydroxyl group and a chloride counterion. The trimethylammonium moiety imparts high solubility in aqueous and polar organic solvents, while the chloro substituent enables further functionalization via nucleophilic displacement. Bench-stable under standard conditions, it serves as a versatile intermediate in asymmetric synthesis and phase-transfer catalysis.
(S)-3-Chloro-2-hydroxy-N,N,N-trimethylpropan-1-aminium chloride serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to stereodefined amino alcohol scaffolds. Its quaternary ammonium functionality enhances solubility and facilitates purification, while the pendant hydroxyl and chloro groups support orthogonal transformations in medicinal chemistry workflows. The compound exhibits excellent bench stability and functions reliably in standard coupling and functionalization reactions.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: