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Structure of 936030-54-5
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This imidazolium salt features a 3-allyl and 1-vinyl substitution pattern on the imidazole core, delivering enhanced reactivity in cationic polymerization. The tetrafluoroborate anion ensures high solubility in polar solvents and facilitates efficient catalytic turnover. Bench-stable under standard conditions, it enables streamlined synthesis of functionalized polymers through controlled vinyl addition chemistry.
3-Allyl-1-vinyl-1H-imidazol-3-ium tetrafluoroborate serves as a versatile ionic building block for constructing functionalized imidazole scaffolds. Its dual unsaturated substituents enable efficient [3+2] cycloadditions and transition-metal-catalyzed couplings, facilitating rapid access to complex heterocyclic architectures. The tetrafluoroborate counterion ensures excellent bench stability and ease of handling, while the cationic core exhibits favorable functional group tolerance in standard synthetic workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: