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Structure of 42872-83-3
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2-Bromo-5-methylbenzonitrile features a strategically positioned bromine atom and nitrile group on a methyl-substituted benzene ring, enabling direct functionalization in cross-coupling reactions. The electron-withdrawing nitrile enhances reactivity at the ortho-brominated site, while the methyl group provides steric and electronic modulation. This compound serves as a key intermediate in pharmaceutical and agrochemical synthesis, offering predictable regioselectivity under standard conditions.
2-Bromo-5-methylbenzonitrile serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable aryl bromide and nitrile functionalities. The methyl group provides ortho-directing capability for electrophilic substitution, while the nitrile group offers compatibility with subsequent transformations such as hydrolysis or reduction. Bench-stable and readily purified by recrystallization, it functions efficiently in the construction of heterocyclic scaffolds and functionalized biaryls common in medicinal chemistry research.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: