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Structure of 617709-79-2
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Methyl 5-formyl-1-isopropyl-1H-pyrazole-3-carboxylate features a reactive aldehyde group at the 5-position paired with a sterically hindered isopropyl substituent, enabling selective transformations in heterocyclic synthesis. This bench-stable scaffold integrates readily into medicinal chemistry campaigns requiring modular pyrazole-based building blocks.
Methyl 5-formyl-1-isopropyl-1H-pyrazole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrazole scaffolds. The orthogonally functionalized core—combining a formyl group at C5 and an ester at C3—facilitates diverse transformations including nucleophilic additions, condensations, and metal-catalyzed couplings. Its bench-stable nature and compatibility with common protecting group strategies streamline purification and downstream derivatization in medicinal chemistry and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: