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Structure of 1023971-89-2
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2-Bromo-6-fluoro-4-methylbenzonitrile features a trifunctional aromatic core with bromine, fluorine, and nitrile groups positioned for orthogonal reactivity. The electron-deficient ring facilitates palladium-catalyzed cross-coupling, while the methyl group provides steric stabilization. This bench-stable intermediate enables efficient access to complex heterocycles in medicinal chemistry and materials synthesis.
2-Bromo-6-fluoro-4-methylbenzonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The nitrile group provides a handle for downstream functionalization, while the methyl and fluorine substituents enhance metabolic stability and modulate electronic properties. Its bench-stable nature and compatibility with standard synthetic workflows facilitate efficient access to complex heterocyclic scaffolds and API 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-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: