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Structure of 40180-80-1
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1-(3-Bromo-4-methylphenyl)ethan-1-one features a brominated aromatic ring fused to a ketone-bearing ethyl side chain, delivering a sterically accessible platform for cross-coupling reactions. The para-methyl group enhances electron density at the ring, while the ortho-bromo substituent enables selective functionalization under palladium catalysis. This structure combines synthetic robustness with high reactivity in transition metal-mediated transformations.
1-(3-Bromo-4-methylphenyl)ethan-1-one serves as a versatile building block in medicinal chemistry and materials synthesis, enabling efficient Suzuki-Miyaura and Negishi couplings due to its stable aryl bromide and ketone functionalities. The methyl group enhances lipophilicity and metabolic stability, while the ketone facilitates downstream transformations such as reductive amination or enolization. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step syntheses of heterocyclic scaffolds and functionalized biaryls.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: