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Structure of 18640-58-9
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1-(4-Bromo-3-nitrophenyl)ethanone features a brominated aromatic ring paired with dual electron-withdrawing nitro and ketone functionalities, enabling direct incorporation into cross-coupling reactions. This bench-stable acylating agent facilitates efficient synthesis of complex aryl ketones under standard conditions.
1-(4-Bromo-3-nitrophenyl)ethanone serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient construction of substituted aromatic scaffolds. Its bromo and nitro groups provide orthogonal handles for palladium-catalyzed cross-coupling and selective reduction, respectively. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic campaigns in API development and target-oriented synthesis.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: