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Structure of 10374-51-3
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5-(Hydroxymethyl)dihydrofuran-2(3H)-one features a reactive hydroxymethyl group appended to a labile dihydrofuranone scaffold, enabling direct functionalization in synthetic sequences. This bifunctional motif integrates seamlessly into complex molecule architectures, particularly in carbohydrate-inspired syntheses and bioactive compound derivatization.
5-(Hydroxymethyl)dihydrofuran-2(3H)-one serves as a versatile synthon in medicinal chemistry, enabling efficient access to bioactive heterocycles through its reactive carbonyl and pendant hydroxymethyl group. The molecule exhibits good bench stability and facilitates selective transformations, including oxidation, derivatization, and cyclization reactions, making it valuable for constructing carbohydrate mimetics and core scaffolds in API 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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: