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Structure of 59042-90-9
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(S)-1-(Pyridin-2-yl)ethan-1-ol features a chiral center adjacent to a pyridine ring, delivering a stereodefined scaffold for asymmetric synthesis. The hydroxyl group enables direct functionalization or derivatization, while the aromatic nitrogen enhances solubility and coordination potential. This bench-stable building block integrates seamlessly into medicinal chemistry campaigns targeting kinase inhibitors and bioactive heterocycles.
(S)-1-(Pyridin-2-yl)ethan-1-ol serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of pyridine-containing pharmaceutical intermediates. Its well-defined stereochemistry and bench-stable nature facilitate reliable incorporation into asymmetric syntheses. The molecule functions as a key precursor for β-arylethanol derivatives and participates effectively in standard functional group interconversions, including oxidation and coupling reactions, with high predictability in multistep sequences.
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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: