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Structure of 18583-54-5
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This bench-stable phosphonium salt features a (2,6-dichlorobenzyl) group tethered to a triphenylphosphonium cation, delivering enhanced solubility in polar organic solvents. The electron-deficient aryl moiety facilitates efficient Wittig-type olefination and acts as a robust precursor in synthesis of phosphine oxides and ylide intermediates.
(2,6-Dichlorobenzyl)triphenylphosphonium chloride serves as a reliable precursor for Wittig-type olefination reactions, enabling the synthesis of stabilized alkenes with high stereoselectivity. The dichlorobenzyl group enhances stability and facilitates purification, while the triphenylphosphonium moiety ensures compatibility with standard base-mediated transformations. This reagent functions effectively in the construction of conjugated systems and complex molecular architectures under mild conditions.
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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-H335
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Precautionary Statements : P261-P280-P304+P340-P405-P501
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Lot numbers can be found on the outside label of a product: