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Structure of 52780-15-1
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3-Bromo-2-methylbenzonitrile features a bromine atom at the meta position relative to a nitrile group, with a methyl substituent ortho to the nitrile. This electron-deficient aromatic scaffold enables direct coupling in palladium-catalyzed cross-coupling reactions. The compound exhibits excellent stability under standard conditions and facilitates efficient functionalization in synthetic sequences requiring regiocontrolled aryl halide intermediates.
3-Bromo-2-methylbenzonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromine site. The nitrile group provides a handle for selective transformations, while the methyl substituent enhances regioselectivity in subsequent functionalizations. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient access to complex heterocyclic scaffolds and drug-like molecules.
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H315-H319-H331-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: