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Structure of 740816-14-2
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This fluorinated triazolo-oxazinium salt features a rigid, electron-deficient core that enhances stability and reactivity in C–H functionalization. The pentafluorophenyl group improves solubility in polar solvents and facilitates participation in transition-metal-catalyzed transformations. Designed for use in synthetic methodology development, it enables efficient access to complex heterocyclic architectures under mild conditions.
(5aS,10bR)-5a,10b-Dihydro-2-(2,3,4,5,6-pentafluorophenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium tetrafluoroborate serves as a stable, bench-ready building block for the synthesis of fluorinated heterocyclic scaffolds. Its pentafluorophenyl group enhances metabolic stability and lipophilicity, while the fused triazolooxazine core enables straightforward functionalization via nucleophilic substitution or transition-metal-catalyzed coupling. The tetrafluoroborate counterion ensures high solubility and ease of purification, making it suitable for iterative synthesis in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05,GHS09
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Signal Word : Danger
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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 : H314-H410
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Precautionary Statements : P260-P264-P273-P280-P301+P330+P331-P304+P340-P363-P391-P405-P501
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Lot numbers can be found on the outside label of a product: