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Structure of 850469-00-0
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This chiral imidazolium salt features a sterically hindered mesityl group and a hydroxy-substituted isoprenoid side chain, enabling precise stereocontrol in catalytic transformations. The hexafluorophosphate counterion ensures high solubility in polar aprotic solvents and enhances stability under standard bench conditions.
(S)-1-(1-Hydroxy-3-methylbutan-2-yl)-3-mesityl-4,5-dihydro-1H-imidazol-3-ium hexafluorophosphate(V) serves as a stable, bench-ready chiral imidazolium salt that facilitates asymmetric C–C bond formation via nucleophilic activation. The mesityl group provides steric shielding and electronic stabilization, while the hydroxy-substituted alkyl chain enables derivatization or in situ generation of reactive intermediates. Functions effectively in transition-metal-free organocatalytic transformations and offers excellent solubility and purification compatibility in standard synthetic 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: