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Structure of 191980-54-8
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4-Iodo-1-trityl-1H-pyrazole features a trityl-protected pyrazole core with a reactive iodo substituent, enabling selective C–H functionalization. The trityl group provides steric shielding and enhanced solubility, while the iodine serves as a handle for palladium-catalyzed cross-coupling reactions under standard conditions. This derivative supports efficient access to complex heterocyclic scaffolds in synthetic organic chemistry.
4-Iodo-1-trityl-1H-pyrazole serves as a robust building block for the synthesis of functionalized pyrazole scaffolds in medicinal chemistry and catalytic cross-coupling workflows. The trityl group provides excellent stability and facilitates purification, while the iodide enables reliable Suzuki-Miyaura and Stille coupling reactions. Its bench-stable nature and orthogonal reactivity make it ideal for late-stage diversification in complex molecule assembly.
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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-H320-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: