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Structure of 4009-98-7
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(Methoxymethyl)triphenylphosphonium chloride is a Wittig reagent that reacts with aldehydes and ketones to give substituted alkenes. This Wittig reaction finds application as the key step in the synthesis of:Antimalarial drug, (+)-artemisinin.Substituted quinolines.Akuammiline alkaloid picrinine.7H-pyrrolo[2,3-d]pyrimidine derivatives for signal transducers and activators of transcription 6 (STAT6) inhibitors.
(Methoxymethyl)triphenylphosphonium chloride serves as a stable, bench-ready Wittig reagent precursor, enabling efficient synthesis of terminal alkenes from aldehydes. Its methoxymethyl group enhances solubility and simplifies purification, while the triphenylphosphonium moiety ensures high-yielding olefination under standard conditions. Functions reliably in diverse synthetic workflows requiring stereoselective alkene formation.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H411
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Precautionary Statements : P264-P270-P273-P280-P302+P352-P330-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: