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Structure of 35034-22-1
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2-Methyl-1H-imidazole-5-carbaldehyde delivers a reactive aldehyde group flanked by an electron-rich imidazole scaffold, enabling direct incorporation into heterocyclic architectures. This bench-stable compound facilitates efficient coupling reactions in synthetic and medicinal chemistry workflows.
2-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 reductive amination, Grignard additions, and coupling reactions with nucleophiles, while the electron-rich imidazole core exhibits favorable stability under mild reaction conditions. The methyl substituent enhances solubility and aids in purification, making it well-suited for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: