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Structure of 6575-10-6
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2-Chloro-6-methoxybenzonitrile features a strategically positioned nitrile group flanked by chlorine and methoxy substituents, enabling precise electronic tuning for cross-coupling reactions. This bench-stable, moisture-tolerant aryl building block integrates efficiently into pharmaceutical intermediates and functional materials, offering enhanced reactivity in palladium-catalyzed transformations under standard conditions.
2-Chloro-6-methoxybenzonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinolines, and other heterocyclic scaffolds via nucleophilic aromatic substitution or palladium-catalyzed coupling. Its ortho-chloro and para-methoxy substituents provide complementary reactivity and electronic modulation, while the nitrile group offers a robust handle for further functionalization. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for high-throughput screening and process development workflows.
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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: