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Structure of 74111-21-0
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(1S,2S)-2-Aminocyclohexanol is a chiral cyclohexanol derivative featuring a primary amine group in the cis-configuration relative to the hydroxyl moiety. This stereochemically defined scaffold delivers enhanced diastereoselectivity in asymmetric synthesis, particularly in catalytic amination and cyclization reactions. The molecule's dual functional groups—bearing both nucleophilic amine and hydrogen-bonding hydroxyl—enable precise molecular recognition and stabilization of transition states. Bench-stable and readily handled under standard conditions, it serves as a high-performance building block for complex natural product and pharmaceutical intermediates.
(1S,2S)-2-Aminocyclohexanol serves as a chiral building block for asymmetric synthesis, enabling stereoselective transformations in medicinal chemistry and catalytic processes. Its bench-stable nature and dual functionality—primary amine and hydroxyl groups—facilitate diverse derivatization, including protection strategies and coupling reactions. The defined stereochemistry supports predictable reactivity in the construction of bioactive heterocycles and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: