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Structure of 68282-52-0
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2,4-Dimethyl-1H-imidazole-5-carbaldehyde features a sterically hindered imidazole core with electron-rich methyl groups flanking a reactive aldehyde handle. This configuration enables efficient coupling in C–H functionalization and transition-metal-catalyzed cross-coupling reactions. The bench-stable, moisture-tolerant aldehyde integrates readily into complex heterocyclic architectures under standard conditions.
2,4-Dimethyl-1H-imidazole-5-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to imidazole-based scaffolds via standard condensation and coupling reactions. Its aldehyde functionality offers high reactivity in nucleophilic addition processes, while the methyl substituents enhance bench stability and facilitate purification. This compound functions effectively in the construction of bioactive molecules and functional materials, particularly where electron-rich imidazoles are required.
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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: