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Structure of 96385-23-8
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(Fluoromethyl)triphenylphosphonium tetrafluoroborate delivers a fluoromethyl group with high electrophilicity and stability under standard conditions. This reagent enables direct fluoromethylation in synthetic transformations, combining ease of handling with reliable reactivity. The tetrafluoroborate counterion enhances solubility and facilitates clean reaction profiles in polar media.
(Fluoromethyl)triphenylphosphonium tetrafluoroborate serves as a reliable source of the fluoromethyl cation, enabling direct fluoromethylation of nucleophiles under mild conditions. Its bench-stable solid form facilitates handling, while broad functional group tolerance supports its use in late-stage modifications. The reagent functions effectively in C–H fluoromethylation and heterocycle synthesis, offering predictable reactivity and clean reaction profiles ideal for medicinal chemistry workflows.
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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: