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Structure of 57381-37-0
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2-Bromo-5-chlorobenzonitrile features a dual halogen substitution pattern on the benzene ring, delivering enhanced reactivity in cross-coupling and nucleophilic aromatic substitution reactions. The nitrile group provides a polar handle for downstream functionalization, while the electron-deficient aromatic core ensures compatibility with palladium-catalyzed transformations under standard conditions.
2-Bromo-5-chlorobenzonitrile serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its compatible halogen substituents. The nitrile group provides a handle for downstream functionalization, while the ortho-bromo and meta-chloro positions offer regioselective reactivity. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for constructing complex heterocycles and pharmaceutical scaffolds.
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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: