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Structure of 1261776-03-7
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2-Bromo-4-iodobenzonitrile features a dual halogen substitution pattern enabling efficient cross-coupling reactions. The nitrile group provides a polar handle for further functionalization, while the bromine and iodine sites offer orthogonal reactivity in palladium-catalyzed transformations. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced pharmaceutical scaffolds.
2-Bromo-4-iodobenzonitrile serves as a versatile biaryl building block in cross-coupling chemistry, enabling efficient access to substituted phenyl nitriles via Pd-catalyzed reactions. The bromo and iodo groups offer orthogonal reactivity for sequential functionalization, while the nitrile moiety provides a handle for downstream transformations. Bench-stable and compatible with standard Suzuki, Stille, and Negishi protocols, it facilitates rapid assembly of complex scaffolds in medicinal chemistry and materials science.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: