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Structure of 3391-30-8
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2,2-Dimethyl-1,3-dioxan-5-ol features a stable cyclic acetal core with a terminal hydroxyl group, enabling direct use in glycosylation chemistry. The geminal dimethyl substitution enhances steric protection and resistance to acid-catalyzed hydrolysis. This bench-stable derivative serves as a reliable building block for carbohydrate synthesis and protected alcohol transformations under standard conditions.
2,2-Dimethyl-1,3-dioxan-5-ol serves as a stable, bench-ready synthon for stereoselective transformations in carbohydrate and heterocyclic synthesis. Its rigid cyclic structure provides predictable stereochemical control, while the hydroxyl group enables selective derivatization under standard conditions. The molecule functions effectively as a protected diol equivalent and participates reliably in coupling reactions with broad functional group tolerance.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: