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Structure of 179692-08-1
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Ethyl 4-iodo-1H-pyrazole-5-carboxylate features a pyrazole core with orthogonal functional handles: a sterically accessible iodide at C4 and an ester group at C5. This combination enables seamless cross-coupling reactions and downstream derivatization under standard conditions, facilitating rapid access to diverse heterocyclic scaffolds in medicinal chemistry and materials synthesis.
Ethyl 4-iodo-1H-pyrazole-5-carboxylate serves as a versatile building block for the synthesis of functionalized pyrazole scaffolds. The iodine substituent enables palladium-catalyzed cross-coupling reactions, while the ester group supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it suitable for iterative synthetic strategies in medicinal chemistry and agrochemical development.
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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: