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Structure of 368869-86-7
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1-(4-Iodophenyl)-1H-pyrazole features a pyrazole core linked to an iodinated phenyl group, enabling direct use in palladium-catalyzed cross-coupling reactions. The iodine moiety serves as a reactive handle for C–C bond formation, while the pyrazole ring imparts stability and polarity. This compound is bench-stable and compatible with standard coupling conditions, facilitating efficient access to biaryl architectures in medicinal chemistry and materials science.
1-(4-Iodophenyl)-1H-pyrazole serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient access to biaryl architectures. Its iodine functionality exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the pyrazole ring provides moderate stability and favorable solubility for bench-scale synthesis. The molecule functions effectively as a key intermediate in constructing heterocyclic scaffolds relevant to 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-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: