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Structure of 886061-26-3
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This chiral amino alcohol features a (S)-configured stereocenter flanked by a 4-chlorophenyl group and a hydroxymethyl moiety, delivering high enantioselectivity in asymmetric synthesis. The pendant hydroxyl and primary amine groups enable efficient derivatization, while the electron-withdrawing chlorine enhances reactivity in transition-metal-catalyzed transformations. Bench-stable under standard conditions, it serves as a key building block for bioactive molecules and functional materials.
(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol serves as a key chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry. Its well-defined stereochemistry and compatibility with standard functional group manipulations enable reliable access to pharmaceutically relevant scaffolds. The molecule exhibits bench stability and facilitates efficient derivatization via amine and hydroxyl groups, supporting diverse coupling and protection strategies in multi-step syntheses.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: