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Structure of 18289-89-9
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(R)-Methyl 2,3-dihydroxypropanoate features a chiral diol motif with defined stereochemistry at C2 and C3, enabling selective incorporation into complex carbohydrate analogs. This bench-stable derivative delivers high stereoselectivity in glycosylation cascades and serves as a key building block for natural product synthesis and glycomimetic development.
(R)-Methyl 2,3-dihydroxypropanoate serves as a key chiral building block in the synthesis of bioactive molecules and natural product analogs. Its well-defined stereochemistry enables reliable incorporation into complex scaffolds, while the diol functionality offers orthogonal reactivity for selective derivatization. The compound exhibits excellent bench stability and facilitates efficient purification, making it a practical choice for medicinal chemistry campaigns and process development.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: