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Structure of 615-34-9
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Methyl 2,3-dihydroxypropanoate is a diol-containing ester featuring two adjacent hydroxyl groups on a three-carbon chain, enabling versatile functionalization in carbohydrate chemistry and bioconjugation. This bench-stable derivative facilitates selective protection strategies and serves as a key intermediate in the synthesis of glycosidic analogs and chiral building blocks.
Methyl 2,3-dihydroxypropanoate serves as a versatile diol-containing building block for the synthesis of carbohydrate mimetics and chiral intermediates. Its two adjacent hydroxyl groups enable selective protection and oxidation sequences, while the ester functionality supports downstream transformations such as reduction or nucleophilic displacement. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, facilitating integration into multi-step synthetic workflows.
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Lot numbers can be found on the outside label of a product: