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Structure of 1401068-25-4
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2-Bromo-4-iododibenzofuran features a sterically hindered dibenzofuran core with complementary halogen substituents, enabling selective cross-coupling reactions under palladium catalysis. The bromine and iodine positions facilitate sequential functionalization, while the planar aromatic system enhances stability and solubility in organic solvents. This compound serves as a key intermediate in the synthesis of conjugated materials for optoelectronic applications.
2-Bromo-4-iododibenzofuran serves as a versatile building block for the synthesis of functionalized dibenzofuran scaffolds via palladium-catalyzed cross-coupling reactions. The orthogonal halogen reactivity enables sequential functionalization, with bromine typically participating in Suzuki or Stille couplings, while the iodine site undergoes efficient Negishi or Sonogashira transformations. Its bench-stable crystalline form and high purity facilitate reproducible, multi-step synthetic sequences in medicinal chemistry and materials science applications.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: