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Structure of 3031-98-9
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This tetrahydroxylated oxohexanoate ester features a stereochemically defined core with hydroxyl groups at C3, C4, C5, and C6, enabling precise engagement in glycosylation reactions. The methyl ester facilitates handling and integration into complex carbohydrate synthesis workflows.
(3S,4R,5S)-Methyl 3,4,5,6-tetrahydroxy-2-oxohexanoate serves as a key chiral building block for the synthesis of complex carbohydrate derivatives and natural product scaffolds. Its defined stereochemistry enables stereoselective glycosylation reactions and facilitates access to polyhydroxylated heterocycles. The molecule exhibits good bench stability and is compatible with standard protecting group strategies, making it suitable for multi-step synthetic sequences in medicinal chemistry and carbohydrate chemistry applications.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: