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Structure of 17289-26-8
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1-Methyl-1H-imidazole-4-carbaldehyde features a reactive aldehyde group flanked by a methyl-substituted imidazole scaffold, enabling direct incorporation into heterocyclic architectures. This bench-stable derivative offers enhanced solubility in polar solvents and serves as a key intermediate for bioactive molecule synthesis.
1-Methyl-1H-imidazole-4-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 or hydrazines under mild conditions. The methyl group enhances solubility and stability, while the imidazole core provides favorable electronic properties for further functionalization. This compound functions reliably in multistep syntheses requiring orthogonal reactivity and is amenable to purification by standard chromatographic methods.
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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: