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Structure of 1431323-18-0
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This bench-stable triazolo-oxazinium salt features a sterically hindered 1-methylethyl group and a pentafluorophenyl moiety, enabling efficient coupling in transition-metal-catalyzed cross-coupling reactions. The tetrafluoroborate counterion enhances solubility and reactivity under standard conditions.
(5S)-5,6-Dihydro-5-(1-methylethyl)-2-(2,3,4,5,6-pentafluorophenyl)-8H-1,2,4-triazolo[3,4-c][1,4]oxazinium tetrafluoroborate serves as a stable, bench-ready building block for the synthesis of fluorinated heterocyclic scaffolds. Its pentafluorophenyl group enables efficient cross-coupling reactions, while the triazolo-oxazine core provides a rigid, electron-deficient platform for medicinal chemistry applications. The tetrafluoroborate counterion enhances solubility and facilitates purification.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: