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Structure of 39021-62-0
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1-Methyl-1H-imidazole-5-carbaldehyde features a conjugated aldehyde group flanked by a methyl-substituted imidazole ring, delivering enhanced stability and solubility in polar solvents. This electronic configuration enables efficient coupling in transition-metal-catalyzed transformations and facilitates direct functionalization at the aldehyde site.
1-Methyl-1H-imidazole-5-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to imidazole-based scaffolds through standard carbonyl transformations. Its aldehyde functionality facilitates nucleophilic additions, reductive aminations, and condensation reactions with amines and hydrazines, while the methylated imidazole ring ensures good bench stability and compatibility with diverse reaction conditions. The compound functions effectively in the construction of bioactive molecules and offers straightforward purification due to its crystalline nature and predictable chromatographic behavior.
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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-H317-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P272-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: