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Structure of 1218791-05-9
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5-(tert-Butyl)-3-iodo-1H-pyrazole features a sterically shielded tert-butyl group at the 5-position, enhancing stability and solubility in organic media. The iodine substituent at the 3-position enables efficient coupling in palladium-catalyzed cross-coupling reactions. This bench-stable pyrazole derivative serves as a key building block for functionalized heterocycles in medicinal chemistry and materials science.
5-(tert-Butyl)-3-iodo-1H-pyrazole serves as a versatile building block for constructing substituted pyrazole scaffolds in medicinal chemistry and materials science. The iodine atom enables reliable cross-coupling reactions, while the tert-butyl group enhances steric stability and facilitates purification. This compound exhibits excellent bench stability and functional group tolerance, making it well-suited for iterative synthesis workflows and scalable applications in heterocyclic chemistry.
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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: