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Structure of 16740-73-1
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This brominated acetophenone derivative features a methoxy-substituted aryl ring and a reactive ketone group, enabling direct integration into cross-coupling and functionalization workflows. The para-bromo substitution enhances electrophilicity for palladium-catalyzed reactions, while the methoxy group provides moderate electron donation and improved solubility in polar organic solvents.
1-(5-Bromo-2-methoxyphenyl)ethan-1-one serves as a versatile building block in cross-coupling reactions and heterocycle synthesis, enabling efficient construction of biaryl and substituted aromatic scaffolds. The bromo group facilitates palladium-catalyzed coupling, while the methoxy functionality offers moderate electron-donating character and orthogonal handle for further modification. Bench-stable and readily purified by column chromatography, it functions reliably in standard synthetic workflows for 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#: 3261
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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 : P260-P280-P301+P330+P331
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Lot numbers can be found on the outside label of a product: