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Structure of 1646-53-3
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3-Bromo-1,2,4,5-tetramethylbenzene features a sterically hindered aromatic core with four methyl groups and a bromine substituent at the 3-position. This configuration enhances stability and facilitates selective coupling reactions in transition-metal-catalyzed transformations. The molecule’s electron-rich framework supports efficient cross-coupling under mild conditions.
3-Bromo-1,2,4,5-tetramethylbenzene serves as a versatile aryl halide building block in cross-coupling reactions, particularly Suzuki and Stille couplings, due to its stability and defined substitution pattern. The bromine substituent enables reliable functionalization under standard catalytic conditions, while the tetramethyl groups provide steric shielding and enhance solubility. Its bench-stable nature and predictable reactivity make it well-suited for iterative synthesis of complex aromatic scaffolds and pharmaceutical intermediates.
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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: