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Structure of 37493-16-6
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(S)-1-Chloropropan-2-ol is a chiral synthetically valuable intermediate featuring a stereodefined secondary alcohol and adjacent chlorine atom. This configuration enables selective transformations in asymmetric synthesis, particularly in the construction of enantiopure pharmaceuticals and agrochemicals. The molecule exhibits favorable reactivity under standard conditions, integrating readily into nucleophilic substitution and elimination cascades.
(S)-1-Chloropropan-2-ol serves as a chiral building block for the synthesis of pharmaceutical intermediates and asymmetric catalysts. Its well-defined stereochemistry enables stereoselective transformations, while its hydroxyl and chloride functionalities offer orthogonal reactivity for downstream functionalization. The compound exhibits good bench stability and facilitates efficient purification, making it suitable for scale-up in medicinal chemistry workflows.
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GHS No : GHS02,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 : H226-H332-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P260-P261-P264-P271-P280-P302+P352-P303+P361+P353-P304+P340-P304+P341-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P370+P378-P403+P233-P403+P235-P405-P501
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Lot numbers can be found on the outside label of a product: