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Structure of 20461-89-6
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1,3-Dithiane-2-carboxylic acid features a stabilized carbanion at the C2 position, enabling direct functionalization in organometallic transformations. The dithiane ring provides exceptional bench stability and moisture tolerance, while the carboxylic acid group offers a handle for derivatization. This combination facilitates efficient synthesis of complex heterocycles and carbonyl-containing compounds under mild conditions.
1,3-Dithiane-2-carboxylic acid serves as a versatile synthon in organic synthesis, enabling the formation of carbon–carbon bonds via dithiane-stabilized carbanions. Its well-established reactivity facilitates alkylation and subsequent functionalization under mild conditions, making it a reliable building block for complex molecular architectures. The molecule exhibits good bench stability and compatibility with common protecting group strategies, supporting efficient purification and integration into multi-step synthetic sequences.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: