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Structure of 19210-21-0
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(S)-2-Chloropropan-1-ol is a chiral synthon featuring a stereodefined hydroxyl group and a chlorine atom at the adjacent carbon. This configuration enables selective transformations in asymmetric synthesis, particularly in nucleophilic substitution and coupling reactions. The molecule exhibits enhanced reactivity compared to its racemic counterpart due to defined stereochemistry, making it valuable for constructing enantiopure intermediates in pharmaceutical and agrochemical development.
(S)-2-Chloropropan-1-ol serves as a chiral building block for stereoselective synthesis, enabling efficient access to functionalized intermediates via nucleophilic substitution. Its bench-stable nature and well-defined stereochemistry facilitate reliable incorporation into pharmaceutical and agrochemical scaffolds. Functions effectively in coupling reactions and as a precursor for heterocyclic ring formation under standard conditions.
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 2611
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Class : 6.1 (3)
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Packing Group : Ⅱ
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Hazard Statements : H226-H302+H312+H332-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P370+P378-P501
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Lot numbers can be found on the outside label of a product: