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Structure of 117007-77-9
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5-Chloro-1-methyl-1H-pyrazole-4-carbaldehyde features a reactive aldehyde group flanked by a chlorinated pyrazole ring and a methyl substituent, enabling direct coupling in heterocyclic synthesis. This bench-stable scaffold integrates readily into pharmaceutical intermediates and functional materials, offering enhanced solubility and electronic tuning for targeted applications.
5-Chloro-1-methyl-1H-pyrazole-4-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to heterocyclic scaffolds via nucleophilic addition and condensation reactions. The aldehyde functionality facilitates coupling with amines, hydrazines, and other nucleophiles under mild conditions, while the chloro and methyl substituents provide orthogonal handles for further functionalization. Bench-stable and readily purified by flash chromatography, it functions effectively in multistep synthesis 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: