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Structure of 1803485-14-4
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This chiral alcohol features a (S)-1-methylpyrrolidin-2-yl group attached to a stereodefined ethanediol scaffold, delivering a rigid, electron-rich moiety ideal for asymmetric synthesis. The pendant hydroxyl enables facile derivatization, while the pyrrolidine ring imparts enhanced solubility and metabolic stability. This configuration supports high enantioselectivity in catalytic transformations.
(S)-1-((S)-1-Methylpyrrolidin-2-yl)ethan-1-ol serves as a chiral building block for the synthesis of bioactive molecules, leveraging its stereogenic centers to direct asymmetric transformations. The molecule exhibits bench stability and facilitates efficient functional group interconversions, enabling straightforward incorporation into complex scaffolds. Its pyrrolidine core provides favorable solubility and compatibility in standard coupling reactions, making it a practical choice for medicinal chemistry and process development workflows.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: