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Structure of 1241678-53-4
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This chiral amine features a (S)-configured stereocenter adjacent to a 4-bromo-3-fluorophenyl group, delivering high enantioselectivity in asymmetric synthesis. The electron-deficient aromatic ring enhances reactivity in transition-metal-catalyzed couplings, while the primary amine facilitates efficient derivatization. Bench-stable and moisture-tolerant, it serves as a key building block for bioactive molecules in medicinal chemistry.
(S)-1-(4-Bromo-3-fluorophenyl)ethanamine serves as a key chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry. Its well-defined stereochemistry and compatible functional groups enable efficient incorporation into diverse scaffolds via standard coupling reactions. The bromo and fluoro substituents provide orthogonal handles for further derivatization, including palladium-catalyzed cross-couplings and nucleophilic substitutions. Bench-stable and readily purified by standard methods, it functions reliably in multi-step syntheses requiring high enantiomeric purity.
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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#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P280-P301+P330+P331
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Lot numbers can be found on the outside label of a product: