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Structure of 69383-59-1
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1-Bromo-2,4-dimethyl-5-nitrobenzene features a nitro group at the para position relative to bromine, enhancing electrophilic reactivity in cross-coupling reactions. The methyl substituents provide steric and electronic modulation, improving stability and solubility under standard conditions. This aryl halide serves as a key building block for functionalized arenes in medicinal chemistry and materials science.
1-Bromo-2,4-dimethyl-5-nitrobenzene serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions such as Suzuki and Stille couplings. The bromo group exhibits high reactivity under standard conditions, while the nitro and methyl substituents provide electronic modulation and steric control. This compound offers excellent bench stability and facilitates efficient functionalization in the construction of substituted aromatic scaffolds relevant to agrochemicals 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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: