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Structure of 1932281-42-9
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(R)-1,4-Dioxane-2-carboxylic acid features a chiral, bench-stable scaffold with a carboxylic acid group at the 2-position of a saturated dioxane ring. This configuration enables selective incorporation into bioactive molecules and synthetic intermediates requiring defined stereochemistry. The compound's stability under standard conditions supports reliable handling in process development workflows.
(R)-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 excellent bench stability and compatibility with standard synthetic transformations, facilitating efficient access to complex molecular architectures 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: