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Structure of 75772-01-9
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This bench-stable phosphonium salt features a benzyl-protected methylene group flanked by triphenylphosphine, enabling efficient Wittig-type olefination under mild conditions. The chloride counterion enhances solubility in polar aprotic solvents, facilitating smooth reaction initiation and consistent yields in synthetic sequences requiring stable, handleable ylide precursors.
((Benzyloxy)methyl)triphenylphosphonium chloride serves as a reliable Wittig reagent precursor, enabling efficient synthesis of allylic and homoallylic alcohols via stabilized ylide formation. Its bench-stable solid form facilitates handling and purification, while the benzyloxy group provides orthogonal protection compatibility in complex molecule assembly. Functions effectively in standard carbonyl olefination protocols with high stereoselectivity and minimal side reactions.
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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: