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Structure of 1821739-82-5
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(S)-1,4-Dioxane-2-carboxylic acid features a chiral, bench-stable dioxane ring with a carboxylic acid group at the 2-position, enabling direct incorporation into asymmetric synthesis. This configuration delivers predictable stereocontrol in cyclization and coupling reactions. The compound's stability under standard conditions facilitates handling and integration into multi-step sequences without racemization.
(S)-1,4-Dioxane-2-carboxylic acid serves as a valuable chiral building block in medicinal chemistry, offering a rigid, oxygenated heterocyclic scaffold with defined stereochemistry. Its carboxylic acid functionality enables direct derivatization into amides, esters, and other bioactive motifs, while the dioxane ring provides metabolic stability and favorable solubility. The compound exhibits bench stability and compatibility with standard coupling protocols, facilitating integration into complex molecule synthesis.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: