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Structure of 2252-45-1
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(3-Bromophenyl)(trifluoromethyl)sulfane features a brominated phenyl ring coupled to a trifluoromethylthio group, delivering enhanced lipophilicity and metabolic stability. This sulfane moiety enables direct incorporation into complex molecular architectures via cross-coupling reactions. The compound exhibits robust bench stability and compatibility with palladium-catalyzed transformations under standard conditions.
(3-Bromophenyl)(trifluoromethyl)sulfane serves as a versatile building block in cross-coupling chemistry, enabling efficient C–S bond formation and facilitating the introduction of trifluoromethylthio groups into aromatic scaffolds. Its bromo substituent supports palladium-catalyzed coupling reactions, while the sulfane functionality offers enhanced stability and orthogonal reactivity. The molecule exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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#: 1760
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314-H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: